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Diseases » Mikaelian syndrome » Glossary
 

Glossary for Mikaelian syndrome

  • Camptodactyly: A rare syndrome characterized mainly by camptodactyly, tall stature and hearing loss. The hearing loss starts at birth or during infancy and progresses during childhood resulting in mild to severe hearing impairment.
  • Camptodactyly, tall stature, and hearing loss syndrome: A rare syndrome characterized mainly by camptodactyly, tall stature and hearing loss. The hearing loss starts at birth or during infancy and progresses during childhood resulting in mild to severe hearing impairment.
  • Coarse hair: The occurrence of coarse feeling hair
  • Dental caries: A destructive process causing decalcification of the tooth enamel leading to cavitation of the tooth
  • Dental conditions: Conditions that affect ones dentition
  • Ear and Hearing conditions: Medical conditions affecting the ears or the hearing systems.
  • Failure To Thrive: Slow growth or inadequate weight gain of an infant or child.
  • Freeman-Sheldon Syndrome: A very rare genetic disorder characterized by abnormal development of the skeleton and muscles.
  • Gordon Syndrome: A genetic musculoskeletal disorder characterized mainly by camptodactyly, cleft palate and club foot. The type and severity of symptoms is variable.
  • Hair conditions: Any disorder the affects the hair
  • Hair loss: Loss or thinning of head or body hair
  • Hand conditions: Any condition that affects the hand
  • Head Conditions: Conditions that affect the head
  • Jacobsen syndrome: A very rare chromosomal disorder involving the absence of a portion of chromosome 11q. The range and severity of symptoms is determined by the size of the portion that is deleted.
  • Kyphoscoliosis: Outward curvature of the spine at the back causing hunching or Dowager's hump
  • Lenz Microphthalmia Syndrome: A condition which is characterized by an abnormally small eye
  • Musculoskeletal conditions: Medical conditions affecting the musculoskeletal system of bones, muscles and related structures.
  • Oculodentodigital syndrome: A rare genetic disorder characterized by small eyes, underdeveloped tooth enamel and permanent flexion of one or more finger joints.
  • Poor growth: Poor body growth or delayed physical development.
  • Sensorineural hearing loss: Hearing loss due to abnormal functioning or damage to the hearing nerve or the cochlea (inner ear) or the part of the brain that processes sound. The hearing problem may be present at birth or may be acquired through such things as aging, excessive noise or diseases such as meningitis.
  • Tel-Hashomer camptodactyly syndrome: A very rare syndrome characterized mainly by finger flexion, facial anomalies, short stature and muscle problems.

 

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