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Symptoms » Large fontanelle » Glossary
 

Glossary for Large fontanelle

Medical terms related to Large fontanelle or mentioned in this section include:

  • 3C syndrome: A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name.
  • Achondroplasia: A rare disease characterized by abnormal bone growth which results in short stature with short arms and legs, large head and characteristic facial features.
  • Adducted thumbs Dundar type: A rare disorder characterized by a thumb abnormality as well as mental retardation, foot defects and other anomalies.
  • Bone symptoms: Symptoms affecting the body's bones
  • Child health symptoms: Symptoms related to pediatric (child) health.
  • Chromosome 1, monosomy 1q25 q32: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as digital defects, facial dysmorphism, retarded growth, mental retardation and spasticity.
  • Chromosome 1, trisomy 1q32 qter: A rare chromosomal disorder where duplication of a portion of chromosome 1 causes various abnormalities such as retarded fetal growth, facial anomalies, mental retardation, stillbirth, heart defects and finger and toe abnormalities.
  • Chromosome 1, trisomy 1q42 qter: A rare chromosomal disorder where duplication of a portion of chromosome 1 causes various abnormalities such as clubfoot, poor muscle tone, neurological dysfunction, short stature, mental retardation and narrowing of the pulmonary arteries and valves.
  • Chromosome 3, monosomy 3q13: A rare chromosomal disorder characterized by a range of abnormalities including facial anomalies, kidney dysfunction, large head, small penis and impaired joint mobility.
  • Cleidocranial dysplasia: A rare genetic disorder characterized by collarbone defects, late ossification of cranial sutures and delayed tooth eruption.
  • Craniolenticulosutural dysplasia: A rare syndrome characterized by skeletal defects and an unusual facial appearance consisting mainly of a prominent forehead, wide-set eyes, broad nose and a prominent forehead with a birthmark.
  • Down Syndrome: A chromosome syndrome causing physical effects and mental retardation.
  • Face symptoms: Symptoms affecting the face
  • Head symptoms: Symptoms affecting the head or brain
  • Hydrocephalus: A condition which is characterized by marked dilatation of the cerebral ventricles
  • Hypopituitarism -- micropenis -- cleft lip palate: A very rare syndrome characterized mainly by low pituitary hormone level, small penis and a cleft lip and palate.
  • Infant symptoms: Symptoms affecting babies and infants.
  • Intrauterine Growth Retardation: Slowly growing fetus in the womb during pregnancy
  • Jequier-Kozlowski-skeletal dysplasia: A very rare syndrome characterized mainly by various skeletal abnormalities and facial anomalies.
  • Kaplan-Plauchu-Fitch syndrome: A very rare syndrome characterized mainly by cone-shaped skull, short stature, deafness and various facial and digital abnormalities.
  • Kosztolanyi syndrome: A very rare syndrome characterized mainly by severely retarded development, long thin fingers, mental retardation and skull and facial abnormalities.
  • Lobstein disease: A group of rare inherited diseases that involves fragile bones. There are many different types based on the severity and extent of symptoms. Some types are severe enough to cause stillbirth or infant death whereas other types may cause few if any problematic symptoms.
  • Macrosomia with lethal microphthalmia: A very rare syndrome characterized mainly by very small eyes and a large body size at birth.
  • Mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia: A very rare syndrome characterized mainly by short stature, abnormal skin pigmentation, small ears and hearing impairment.
  • Mental retardation, X-linked, Wittwer type: A rare disorder characterized by severe mental retardation, retarded growth, seizures and vision and hearing problems. The disorder is inherited in a X-linked manner which means that only males display the full range of symptoms whereas female carriers may have mild or no symptoms.
  • Mesomelia radial hypoplasia bifid thumb unusual facies: A rare syndrome characterized mainly by skeletal abnormalities, dwarfism and hair, nail, skin and teeth abnormalities.
  • Multiple joint dislocations -- metaphyseal dysplasia: A rare disorder characterized by multiple joint dislocations and abnormal bone development as well as various other anomalies.
  • Naguib syndrome: A rare syndrome characterized mainly by wide-set eyes, hypospadias and extra fingers.
  • Osteogenesis imperfecta: Weak bones ("brittle bone disease") and loose joints
  • Rathburn disease: A rare inherited condition involving bone and teeth mineralization abnormalities and reduced phosphatase enzyme activity. The severity of the disorder varies according to the degree of reduction in phosphatase activity.
  • Respiratory symptoms: Symptoms affecting the breathing systems.
  • Retinis pigmentosa -- deafness -- hypogenitalism: A very rare syndrome characterized mainly by progressive retinal damage, deafness and genital anomalies.
  • Rickets: A condition that affects the bones due to vitamin D deficiency
  • Rubella congenital syndrome: The transplacental infection of a fetus with rubella
  • Skeletal symptoms: Symptoms affecting the skeletal system such as the bones.
  • Skull symptoms: Symptoms affecting the skull surrounding the brain.
  • Small baby: Small size of newborn baby
  • Thyroid symptoms: Symptoms affecting the thyroid gland
  • Upton Young syndrome: A syndrome which is characterised by the association of multiple symptoms including mental retardation and multiple nevi

Conditions listing medical symptoms: Large fontanelle:

The following list of conditions have 'Large fontanelle' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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