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Symptoms » Eyelash symptoms » Glossary
 

Glossary for Eyelash symptoms

Medical terms related to Eyelash symptoms or mentioned in this section include:

  • 2p21 deletion syndrome: This syndrome is a more severe form hypotonia-cystinuria syndrome as a larger portion of genetic material from chromosome 2p21 is deleted. It is characterized by infant seizures, reduced muscle tone, developmental delay, lactic acidosis and unusual facial appearance.
  • 2q deletion: A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Ablepharon macrostomia syndrome: A rare disorder involving a number of mainly physical abnormalities.
  • Acrofacial dysostosis Preis type: One of a group of disorders characterized by defective limb and facial development. The Preis type is very rare and the range and severity of symptoms is variable.
  • Acrofacial dysostosis, Palagonia type: One of a group of disorders characterized by defective limb and facial development. The Palagonia type is very rare and the symptoms are relatively mild.
  • Acromicric dysplasia: A rare genetic syndrome characterized by various severe developmental abnormalities of the skeletal bones and facial anomalies.
  • Alopecia immunodeficiency: A rare syndrome characterized by alopecia and primary immunodeficiency.
  • Alopecia mental retardation hypogonadism: A rare syndrome characterized by mental retardation, abnormal gonad functioning and a total lack of hair at birth. After childhood, sparse hair growth may occur.
  • Alopecia universalis: Complete loss of all body hair.
  • Alopecia, epilepsy, pyorrhea, mental subnormality: A rare syndrome characterized by alopecia, epilepsy, mental retardation and pus-producing gum and tooth inflammations.
  • Amaurosis hypertrichosis: A rare syndrome characterized by severe retinal dystrophy and excessive growth of hair.
  • Blepharitis: A common eyelid inflammation
  • Cantú syndrome: A rare syndrome characterized mainly by excessive growth of hair, enlarged heart and abnormal development of bone and cartilage
  • Cartilage Hair Hypoplasia: An inherited disorder characterized by short-limb dwarfism as well as hair that is short, fine, brittle and often light colored.
  • Cerebro-oculo-nasal syndrome: A rare syndrome characterized mainly by eye, nose and brain malformations.
  • Christianson Fourie syndrome: A very rare syndrome characterized mainly by hair and nail abnormalities.
  • Chromosome 1, uniparental disomy 1q12 q21: A rare chromosomal disorder where part or all of the short arm (p) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Chromosome 12, Isochromosome 12p Mosaic: A very rare disorder genetic disorder involving abnormalities in chromosome 12. The severity of symptoms is variable and tends to include a wide range of defects and abnormalities.
  • Chromosome 12p tetrasomy syndrome: A rare chromosomal disorder where there are four copies of the short arm (p) of chromosome 12 rather than the normal two resulting in various abnormalities.
  • Chromosome 13q duplication syndrome: A rare chromosomal disorder where the long arm (q) of chromosome 13 is duplicated resulting in various physical, neurological and developmental abnormalities.
  • Chromosome 16p, partial duplication: A rare chromosomal disorder involving an extra copy of genetic material from the short arm of chromosome 16. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material.
  • Chromosome 16q, partial duplication: A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 16. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material. Severe cases often result in spontaneous abortion or infant death.
  • Chromosome 19q13.11 Deletion syndrome: A rare genetic syndrome involving features such as poor fetal growth, reduced fetal activity, developmental problems and various other physical symptoms.
  • Chromosome 1p deletion syndrome: A rare chromosomal disorder where part or all of the short arm (p) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Chromosome 2, monosomy 2q: A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Chromosome 22 Ring: A rare chromosomal disorder where genetic material from one or both ends of chromosome 22 is missing and the two broken ends have rejoined to form a ring. The resulting type and severity of symptoms is determined by the amount and location of genetic material missing.
  • Chromosome 3, Trisomy 3q2: A rare chromosomal disorder involving the duplication of a portion of the long arm of chromosome 3. The symptoms are determined by the size and exact location of the duplicated portion.
  • Chromosome 7, trisomy 7q: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 7 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
  • Chromosome 7q duplication syndrome: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 7 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
  • Cleft palate, bilateral choanal atresia, curly hair and congenital hypothyroidism: A rare syndrome characterized by the association of curly, choanal atresia, cleft palate and congenital hypothyroidism.
  • Clouston syndrome: A rare genetic ectodermal disorder characterized by skin, hair, nail and eye abnormalities.
  • Coffin-Siris Syndrome: A rare genetic disorder characterized by underdeveloped or absent fifth finger and toenails and coarse facial features.
  • Congenital hypotrichosis milia: A rare inherited disorder characterized by reduced hair from birth and the development of numerous milia which tend to disappear by adolescence. The milia occur on the face, chest, armpits and genital area.
  • Contractures hyperkeratosis lethal: A rare fatal congenital syndrome where numerous abnormalities arise from reduced fetal movement due to excessively tight skin.
  • Cornelia de Lange syndrome 2: A very rare disorder involving delayed physical development and various malformations involving the head, face and limbs. Type 2 is not as severe as type 1 with some of the abnormalities not presenting until later in life or absent altogether. The range and severity of symptoms is variable.
  • Cornelia de Lange syndrome 3: A very rare disorder involving delayed physical development and various malformations involving the head, face and limbs. Type 3 is a very mild form of the disorder and is typified by mildly unusual facial appearance and no skeletal or limb malformations.
  • Craniodigital syndrome -- mental retardation: A very rare syndrome characterized by webbed fingers and toes, mental retardation and skull and facial anomalies.
  • Deafness -- pili torti -hypogonadism: An inherited condition characterized by twisted hairs, hypogonadism and nerve deafness.
  • Deformity symptoms: Various types of deformity
  • Del (2) (q23.3-q24.2): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in the few reported cases. The manifestations linked to most genetic defects are often variable to some degree.
  • Del (2) (q37.1-qter): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in the few reported cases. The manifestations linked to most genetic defects are often variable to some degree.
  • Deletion 2q: A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Deletion of the Short Arm of Chromosome 1: A condition characterized by deletion of the short arm of chromosome 1
  • Developmental problems: Physical or mental development difficulty.
  • Duane anomaly -- mental retardation: A very rare syndrome characterized mainly by mental retardation and eye movement problems (Duane anomaly).
  • Duplication 7q: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 7 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
  • Ectodermal dysplasia -- alopecia -- preaxial polydactyly: A rare syndrome characterized by facial abnormalities, extra toes and sparse or absent hair.
  • Ectodermal dysplasia -- arthrogryposis -- diabetes mellitus: A rare syndrome characterized by diabetes, short stature and tooth, hair and nail abnormalities.
  • Ectodermal dysplasia trichoodontoonychial type: A rare syndrome characterized by nail, tooth and hair abnormalities.
  • Ectodermal dysplasia with natal teeth, Turnpenny type: A rare syndrome characterized mainly by missing teeth, sparse hair and dark velvety skin patches called acanthosis nigricans. The skin patches usually disappears during the second decade and may reoccur during pregnancy.
  • Ectodermal dysplasia, 'pure' hair-nail type: A rare syndrome characterized mainly by greatly reduced hair on the scalp, eyelashes and eyebrows as well as abnormal nails.
  • Ectodermal dysplasia, Margarita type: A rare genetic disorder characterized by mental retardation, webbed digits, cleft lip, cleft palate, sparse hair, reduced sweating and teeth abnormalities. Progressive loss of scalp hair usually results in baldness by adulthood.
  • Ectrodactyly -- Ectodermal Dysplasia -- Cleft Lip/Palate Syndrome, Type 1: EEC (Ectrodactyly, ectodermal dysplasia, cleft lip/palate) is a rare inherited condition characterized by split hand and foot deformities of variable severity, cleft lip or palate and teeth and hair anomalies. There are two main types of EEC which differ in the origin of the genetic defect. Type 1 is caused by a defect on chromosome 7q11. The severity and type of symptoms and deformities is highly variable.
  • Ectrodactyly -- Ectodermal Dysplasia -- Cleft Lip/Palate Syndrome, Type 3: EEC (Ectrodactyly, ectodermal dysplasia, cleft lip/palate) is a rare inherited condition characterized by split hand and foot deformities of variable severity, cleft lip or palate and teeth and hair anomalies. There are two main types of EEC which differ in the origin of the genetic defect. Type 3 is caused by a defect on chromosome 3q27. The severity and type of symptoms and deformities is highly variable.
  • Ectrodactyly ectrodermal dysplasia: A rare genetic disorder characterized by missing digits and hair, teeth and nail abnormalities. The severity of the hand and foot malformations is variable.
  • Ectropion: Outward turning of the eyelid away from the eye.
  • Ehlers-Danlos syndrome, progeroid form: A connective tissue disorder caused by an enzyme (xylosylprotein 4-beta-galactosyl transferase) deficiency.
  • Entropion: A condition in which the eyelids fold inward causing the eyelashes to rub against the eye.
  • Eye pain: Pain in the eye.
  • Eye symptoms: Symptoms affecting the eye
  • Eyebrow Duplication -- Stretchable Skin -- Syndactyly: A rare syndrome characterized by partially duplicated eyebrows, abnormally stretchy skin and webbed digits.
  • Eyebrow symptoms: Symptoms affecting the eyebrows.
  • Eyebrows duplication of, with stretchable skin and syndactyly: A rare syndrome characterized mainly by duplication of some of the eyebrow, increased skin elasticity and webbed fingers and toes.
  • Eyebrows duplication syndactyly: A rare syndrome characterized mainly by duplication of some of the eyebrow, webbed fingers and toes and occasionally increased skin elasticity and other variable symptoms.
  • Eyelash bleeding: Bleeding from the base of the eyelashes - usually occurs due to physical injury.
  • Eyelash blister: Small raised fluid filled lesions seen along the eyelid area.
  • Eyelash bruise: Bruise along the eyelash margin of the eyelids..
  • Eyelash burning sensation: Abnormal burning sensations felt at the base of the eyelashes.
  • Eyelash deformity: Alteration or distortion in the normal appearance of the eyelashes.
  • Eyelash infection: Infection at the base of the eyelashes.
  • Eyelash inflammation: Inflammation at the base of the eyelashes.
  • Eyelash numb: Abnormal sensation of numbness felt at the base of the eyelashes.
  • Eyelash rash: Raised erythematous area along the eyelash.
  • Eyelash spasm: Abnormal contraction of the muscle of the eyelid area.
  • Eyelash symptoms: Symptoms affecting the eyelash
  • Eyelash tingling: Abnormal tingling sensations felt at the base of the eyelashes.
  • Eyelash ulcer: Break in the continuity of the skin along the eyelid area.
  • Eyelash weakness: Weakness in the musculature along the eyelid margins.
  • Eyelid symptoms: Symptoms affecting the eyelid
  • FLOTCH syndrome: A very rare syndrome characterized mainly by kidney stones, completely white nails and cysts that form in oil producing areas of skin.
  • Face symptoms: Symptoms affecting the face
  • Facial ectodermal dysplasia: A very rare inherited disorder characterized by hair, teeth, nail and skin abnormalities. The type and severity of symptoms is variable.
  • Floating Harbor Syndrome: A rare genetic disorder characterized by growth deficiency, typical facial appearance and speech delay.
  • Focal facial dermal dysplasia, type II: A rare inherited disorder characterized by scar-like depressions on the temples due to a lack of fat under the skin as well as eye anomalies.
  • Friedel Heid Grosshans syndrome: A very rare syndrome characterized mainly by kidney stones, completely white nails and cysts that form in oil producing areas of skin.
  • Garret-Tripp syndrome: A rare syndrome characterized mainly by extra digits, a lack of hair and scaly skin on the scalp, face and neck.
  • Glomerulonephritis -- sparse hair -- telangiectases: A rare syndrome characterized by sparse hair, kidney disease and enlarged skin blood vessels (telangiectasia).
  • Goldstein-Hutt syndrome: A rare syndrome characterized mainly by cataracts, excessive eyelash growth and and a blood abnormality (the red blood cells are spherical instead of doughnut shaped which makes them fragile).
  • Hair defect with photosensitivity and mental retardation: A very rare syndrome characterized mainly by mental retardation, sensitivity to light and sparse, fragile hair
  • Hair symptoms: Symptoms affecting the hair
  • Halal Setton Wang syndrome: A very rare syndrome characterized mainly by eye, teeth, nail and skin abnormalities.
  • Hallermann-Streiff Syndrome: A condition which affects stature, head shape and hair growth
  • Head symptoms: Symptoms affecting the head or brain
  • Hidrotic ectodermal dysplasia, type Christianson-Fourie: A very rare syndrome characterized mainly by hair and nail abnormalities.
  • Hypopigmented lesions in children: Hypopigmented lesions in children refers are sores or ulcers that are colorless or have lost color in a child.
  • Hypopituitarism: A condition characterized by diminished hormonal section by the pituitary gland
  • Hypotrichosis -- lymphoedema -- telangiectasia: A rare syndrome characterized mainly by sparse hair, lymphedema and telangiectasia.
  • Ichthyosiform erythroderma, nonbullous congenital: A rare inherited skin disorder characterized by redness, scaling and ultimately thickening of the skin that occurs from birth. The severity of the condition is variable.
  • Ichthyosis, Keratosis Follicularis Spinulosa Decalvans: A rare inherited skin disorder where the skin around hair follicles becomes stiffened and the resulting scarring causes hair loss.
  • Keratosis follicularis -- dwarfism -- cerebral atrophy: A very rare syndrome characterized mainly by dwarfism, brain degeneration and a hair follicle disorder.
  • Keratosis follicularis Spinulosa Decalvans, Autosomal Dominant: A rare inherited skin disorder affecting mostly males and characterized by hardening of skin around hair follicles which leads to scarring and loss of hair. The skin on the face, neck, forearms and other areas can also be affected. Because the condition is inherited in a X-linked manner, carrier females may have milder symptoms.
  • Keratosis follicularis Spinulosa Decalvans, X-Linked: A rare inherited skin disorder affecting mostly males and characterized by hardening of skin around hair follicles which leads to scarring and loss of hair. The skin on the face, neck, forearms and other areas can also be affected.
  • Keratosis follicularis spinulosa decalvans: A rare inherited skin disorder affecting mostly males and characterized by hardening of skin around hair follicles which leads to scarring and loss of hair. The skin on the face, neck, forearms and other areas can also be affected.
  • Leprosy, susceptibility to, 1: A chronic, progressive infectious disease caused by Mycobacterium leprae which causes skin sores and also affects the eyes, mucous membranes and peripheral nerves. The range of manifestations and severity of symptoms is quite variable. Researchers have discovered a number of genetic mutations linked to an increased susceptibility to leprosy. Type 1 is linked to a defect on chromosome 10p13.
  • Leprosy, susceptibility to, 2: A chronic, progressive infectious disease caused by Mycobacterium leprae which causes skin sores and also affects the eyes, mucous membranes and peripheral nerves. The range of manifestations and severity of symptoms is quite variable. Researchers have discovered a number of genetic mutations linked to an increased susceptibility to leprosy. Type 2 is linked to a defect on chromosome 6q25.2-q27.
  • Leprosy, susceptibility to, 3: A chronic, progressive infectious disease caused by Mycobacterium leprae which causes skin sores and also affects the eyes, mucous membranes and peripheral nerves. The range of manifestations and severity of symptoms is quite variable. Researchers have discovered a number of genetic mutations linked to an increased susceptibility to leprosy. Type 3 is linked to a defect on chromosome 4q32 and 4p14.
  • Leprosy, susceptibility to, 4: A chronic, progressive infectious disease caused by Mycobacterium leprae which causes skin sores and also affects the eyes, mucous membranes and peripheral nerves. The range of manifestations and severity of symptoms is quite variable. Researchers have discovered a number of genetic mutations linked to an increased susceptibility to leprosy. Type 4 is linked to a defect on chromosome 6p21.3.
  • Leukonychia totalis -- trichilemmal cysts -- cilliary dystrophy: A very rare syndrome characterized mainly by kidney stones, completely white nails and cysts that form in oil producing areas of skin.
  • Lid and lashes stick together: eyelids may appear sticky due to the inflamed discharge
  • Limb symptoms: Symptoms affecting the limbs
  • Loss of eyelashes: The loss of a persons eyelashes
  • Madokoro-Ohdo-Sonoda syndrome: A rare disorder characterized by the absence of all four limbs, an unusual face and retarded development.
  • Mandibuloacral dysplasia: A very rare syndrome characterized mainly by a prematurely aged appearance and bone abnormalities. There are two subtypes with type B involving loss of fat layers under the skin mainly in the extremities, face and trunk whereas type A involves mainly the extremities. The severity of the symptoms is variable.
  • Mandibuloacral dysplasia with type A lipodystrophy: A very rare syndrome characterized mainly by a prematurely aged appearance and bone abnormalities. Loss of fat layers under the skin occurs mainly in the extremities in type B. The severity of the symptoms is variable.
  • Marie Unna congenital hypotrichosis: A rare inherited condition characterized by hair loss that starts during childhood. Women tend to have normal thickness hair that doesn't grow very long and loss of hair on other parts of the body such as eyelashes. Nail and teeth growth is also usually limited.
  • McKusick type metaphyseal chondrodysplasia: A rare genetic disorder characterized by short stature, skeletal abnormalities and fine, fragile hair.
  • Megarbane-Jalkh Syndrome: A rare condition reported in two related infants and involving a range of abnormalities such as developmental delay, unusual facial features, wrinkled skin, liver failure and fragile bones. One of the infants died before the age of 2 years due to liver failure.
  • Microcephalic osteodysplastic primordial dwarfism types 1 and 3: Microcephalic osteodysplastic primordial dwarfism types 1 and 3 were originally regarded as separate conditions but it was recently concluded that they were different expressions of the same condition. The main differences between the two forms is a difference in the radiological bone anomalies. The condition is characterized mainly by bone abnormalities, short stature and a small head.
  • Moloney syndrome: A very rare syndrome characterized mainly by wasting of the choroids in the eye and sparse, fine hair. The choroid is a layer of blood vessels that lies between the retina and the sclera and delivers blood to the back of the eye.
  • Myxedema: The most severe form of hypothyroidism characterized by swelling of extremities and face.
  • NISCH syndrome: A rare syndrome characterized by sparse scalp hair, scaly skin and inflammation and fibrosis of the bile ducts.
  • Nablus mask-like facial syndrome: A rare disorder characterized by an unusual mask-like facial appearance.
  • Neu-Laxova Syndrome: A rare fatal genetic disorder characterized by microcephaly and multiple congenital abnormalities. Death occurs during the fetal or newborn stage.
  • OFD syndrome type 8: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps and finger abnormalities.
  • Oculo tricho dysplasia: A very rare syndrome characterized mainly by eye, tooth and hair abnormalities
  • Oculomaxillofacial dysostosis: A very rare syndrome characterized mainly by eye, jaw and facial abnormalities.
  • Okamuto Satomura syndrome: A very rare syndrome characterized mainly by kidney, heart and facial abnormalities as well as reduced muscle tone and mental retardation.
  • PARC syndrome: A very rare syndrome characterized mainly by a cleft palate, recessed jaw, alopecia and a mottled skin appearance called poikiloderma.
  • Pallister Killian Mosaic Syndrome: Pallister Killian Mosaic Syndrome is a very rare disorder genetic disorder involving abnormalities in chromosome 12. The severity of symptoms is variable and tends to include a wide range of defects and abnormalities.
  • Pallister Mosaic Syndrome Tetrasomy 12p: A very rare disorder genetic disorder involving abnormalities in chromosome 12. The severity of symptoms is variable and tends to include a wide range of defects and abnormalities.
  • Pallister-Killian Syndrome: A rare genetic disorder due to tetrasomy of the 12th chromosome
  • Pili torti -- developmental delay -- neurological abnormalities: A very rare syndrome characterized mainly by developmental delay, twisted hair shafts and neurological symptoms.
  • Popliteal pterygium syndrome, lethal type: A rare lethal condition characterized by webbing of skin as well as various other physical and mental abnormalities.
  • Progeria: A rare fatal genetic disorder characterized by extremely premature aging.
  • Pseudoprogeria syndrome: A very rare syndrome characterized mainly by absent eyelashes and eyebrows as well a mental retardation.
  • Pterygium, Popliteal, lethal type: A rare lethal condition characterized by webbing of skin as well as various other physical and mental abnormalities.
  • Rombo syndrome: A very rare syndrome characterized mainly by hair anomalies and skin problems.
  • Rubinstein-Taybi Syndrome: A rare congenital disorder characterized by very small stature, broad thumbs and toes, slanted palpebral fissures and hypoplastic maxilla.
  • Satoyoshi syndrome: A very rare syndrome characterized by alopecia, diarrhea, skeletal abnormalities and painful leg cramps caused by physical exercise or emotional stress.
  • Scalp symptoms: Symptoms of the scalp on the head
  • Schwartz-Jampel Syndrome: A rare genetic disorder characterized by myotonia, blepharophimosis and joint limitation.
  • Scott Craniodigital Syndrome: A condition which is characterized by deformities of the cranium and fingers
  • Scott syndrome: A very rare inherited syndrome characterized by head and digital abnormalities as well as mental retardation.
  • Setleis Syndrome:
  • Siemens syndrome: A rare inherited skin disorder where the skin around hair follicles becomes stiffened and the resulting scarring causes hair loss.
  • Skeletal symptoms: Symptoms affecting the skeletal system such as the bones.
  • Sparse eyelashes: Sparse eyelashes are eyelashes refers to a condition in which there are too few or a lack of eyelashes.
  • Spastic paraplegia -- neuropathy -- poikiloderma: A very rare syndrome characterized mainly by progressive stiffness and weakness of the legs, peripheral nerve degeneration and a skin disorder called poikiloderma. The eyelashes and eyebrows are usually gone by the age of three.
  • Stratton-Parker syndrome: A very rare syndrome characterized by short stature, heart positioned on the wrong side of the chest (dextrocardia) and a bone development anomaly.
  • Styes: inflammation of the glands in the eyelids
  • Sudden onset of stye:
  • Tetra-amelia with ectodermal dysplasia and lacrimal duct abnormalities: A rare disorder involving tear duct abnormalities, missing arms and legs, retarded development and an unusual facial appearance.
  • Total Hypotrichosis, Mari type: A rare inherited form of congenital alopecia (hair loss). It occurs primarily in the Mari population in a part of Russia.
  • Trachoma: Chronic bacterial eye condition in the developing world
  • Trichiasis: inward turning of the eyelids
  • Trichodermodysplasia -- dental alterations: A rare syndrome characterized mainly by hair, skin and tooth abnormalities.
  • Trichodysplasia xeroderma: A rare disorder involving the skin and hair.
  • Trigonocephaly -- bifid nose -- acral anomalies: A rare syndrome characterized mainly by a prominent triangular shaped forehead, short head, bulbous nose, small jaw, large mouth, poor muscle tone and foot abnormalities.
  • Unusual facies and autosomal dominant hypohidrotic ectodermal dysplasia: A rare syndrome characterized mainly by an unusual facial appearance and hair, nail, teeth and sweating abnormalities.
  • Vitiligo: A condition which is characterized by chronic pigmentary changes to the skin seen by white patches
  • Xylosylprotein 4-beta-galactosyltransferase (XGPT) deficiency: A variant of the connective tissue disorder called Ehlers-Danlos. It is caused by a deficiency of galactosyltransferase I.
  • Yunis Varon syndrome: A multisystem genetic disease that affects the skeletal system in particular

Conditions listing medical symptoms: Eyelash symptoms:

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Conditions listing medical complications: Eyelash symptoms:

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