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Symptoms » Widely-spaced teeth » Glossary
 

Glossary for Widely-spaced teeth

Medical terms related to Widely-spaced teeth or mentioned in this section include:

  • Angelman syndrome: A rare genetic disorder characterized by a puppet-like gait, fits of laughter and characteristic facial features.
  • Anonychia: Anonychia is a rare disorder characterized by absence of nails.
  • Anonychia -- microcephaly: A very rare syndrome characterized by the absence of nails and a small head.
  • Brachmann-De Lange Syndrome: A rare congenital disorder characterized by very small stature, synophrys, thin downturning upper lip and micromelia.
  • Breath symptoms: Breath-related symptoms including breath odor
  • Breathing symptoms: Symptoms affecting the breathing systems.
  • Cerebellar ataxia: Cerebellar ataxia is a form of ataxia originating in the cerebellum. Romberg's test can be used to distinguish cerebellar ataxia from other forms of ataxia
  • Cerebellar ataxia -- ectodermal dysplasia: A rare syndrome characterized by balance and coordination problems and teeth and hair abnormalities.
  • Chromosome 17, deletion 17q23 q24: A rare chromosomal disorder involving deletion of genetic material from the long arm of chromosome 17. The type and severity of symptoms are determined by the amount and location of the lost genetic material.
  • Coffin-Lowry syndrome: A rare genetic disorder characterized by down slanting space between eyelids, bulbous nose, soft hands and tapering fingers.
  • Cornelia de Lange syndrome 1: A very rare disorder involving delayed physical development and various malformations involving the head, face and limbs. Type 1 is more severe than type 2 though the range and severity of symptoms is variable.
  • Cranioectodermal dysplasia: A rare condition involving various congenital deformities such as short stature, long head, widely spaced eyes and teeth abnormalities.
  • De Lange 1: A rare disorder involving a variety of congenital abnormalities including retarded growth, behavioral problems, characteristic facial features and upper limb abnormalities.
  • Dental symptoms: Symptoms affecting teeth or mouth area.
  • Developmental problems: Physical or mental development difficulty.
  • Ectodermal dysplasia -- ectrodactyly -- macular dystrophy: A rare syndrome characterized mainly by skin, hair, nail and eye abnormalities as well as missing fingers.
  • Face symptoms: Symptoms affecting the face
  • Hand symptoms: Symptoms affecting the hand
  • Hay-Wells Syndrome: A rare genetic disorder characterized by ankyloblepharon, ectodermal dysplasia, and cleft lip and/or cleft palate.
  • Hay-Wells syndrome, recessive type: A rare recessively inherited genetic disorder characterized by ankyloblepharon, ectodermal dysplasia, and cleft lip and/or cleft palate. The recessive form of this condition is distinguished by the presence at birth of adhesions between the upper and lower jaws.
  • Head symptoms: Symptoms affecting the head or brain
  • Hutchinson incisors: Abnormally shaped permanent front teeth (incisors). The defect is usually associated with congenital syphilis.
  • Large gaps between teeth in children: Large gaps between teeth in children refers to a child who has spaces between the teeth that are bigger than usual.
  • Limb symptoms: Symptoms affecting the limbs
  • Mannosidosis, alpha B lysosomal: A rare inherited metabolic disorder involving a deficiency of an enzyme (alpha-mannosidosase) which results in the accumulation of certain chemicals in the body which leads to progressive damage.
  • Mouth symptoms: Symptoms of the mouth or oral area.
  • Mucopolysaccharidosis type 2 Hunter syndrome- mild form: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of the enzyme (iduronidate 2-sulfatase) needed to break it down.
  • Mucopolysaccharidosis type 2 Hunter syndrome- severe form: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of the enzyme (iduronidate 2-sulfatase) needed to break it down.
  • Mucopolysaccharidosis type 6: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of the enzyme (Arylsulfatase ?) needed to break it down.
  • Oculocerebral hypopigmentation syndrome, type Preus: A very rare syndrome characterized mainly by eye, brain and pigmentation abnormalities.
  • Phenylketonuria: A metabolic disorder where there is a deficiency of the enzyme phenylalanine hydroxylase which leads to a harmful buildup of the phenylalanine in the body. Normally the phenylalanine is converted into tyrosine. The severity of the symptoms can range from severe enough to cause mental retardation to mild enough not to require treatment. Severity is determined by the level of impairment of enzyme activity of phenylalanine hydroxylase.
  • Respiratory symptoms: Symptoms affecting the breathing systems.
  • Scalp -- ear -- nipple syndrome: A very rare syndrome characterized mainly by scalp, nipple and ear abnormalities.
  • Skeletal symptoms: Symptoms affecting the skeletal system such as the bones.
  • Skull symptoms: Symptoms affecting the skull surrounding the brain.
  • TDO type II: A rare genetic ectodermal disorder characterized by kinky hair, tooth enamel and bone abnormalities and differs from type I mainly by a small head and increased long bone density.
  • Teebi-Kaurah syndrome: A very rare syndrome characterized mainly by a small head and absent nails.
  • Teeth pain: Toothache due to infectious or non-infectious etiology.
  • Throat symptoms: Symptoms affecting the throat
  • Tricho-dento-osseous syndrome: A rare genetic disorder characterized by kinky hair, tooth enamel and bone abnormalities. There are two different subtypes with type I being distinguished from type II by the presence of a small head and increased density in the long bones.
  • Tricho-dento-osseous syndrome II:
  • Tricho-dento-osseous syndrome type:
  • Tricho-dento-osseous syndrome type I: A rare genetic ectodermal disorder characterized by kinky hair, tooth enamel and bone abnormalities.
  • XLMR-Hypotonic Facies Syndrome:
  • Zunich-Kaye syndrome: A very rare genetic syndrome characterized by a range of symptoms such as colobomas of the eye, heart defects, ichthyosiform dermatosis, mental retardation and ear defects.

Conditions listing medical symptoms: Widely-spaced teeth:

The following list of conditions have 'Widely-spaced teeth' 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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