Oculodentodigital syndrome: A rare genetic disorder characterized by small eyes, underdeveloped tooth enamel and permanent flexion of one or more finger joints. More detailed information about the symptoms, causes, and treatments of Oculodentodigital syndrome is available below.
See full list of 22 symptoms of Oculodentodigital syndrome
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Research the causes of these diseases that are similar to, or related to, Oculodentodigital syndrome:
See full list of 27 occasional symptoms of Oculodentodigital syndrome
Commonly undiagnosed diseases in related medical categories:
Psoriatic arthritis often undiagnosed cause of joint conditions: Patients with the skin condition psoriasis can also have the related arthritis subtype called "psoriatic arthritis". This arthritic condition tends to be overlooked,...read more »
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Medical research articles related to Oculodentodigital syndrome include:
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The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Oculodentodigital syndrome include:
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Types of Oculodentodigital syndrome
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A syndrome with a variable phenotype marked mainly by eye abnormalities, craniofacial dysmorphism, dental anomalies, hand and foot malformations, various skeletal defects, and mildly delayed mental development. - (Source - Diseases Database)
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