39 top medical experts on Oculocerebral hypopigmentation syndrome type Preus across 7 countries, including 3 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Oculocerebral hypopigmentation syndrome type Preus: Oculocerebral hypopigmentation syndrome, Preus type is a rare congenital syndrome characterized by skin and hair hypopigmentation, growth retardation, and intellectual deficit that are associated with a combination of various additional clinical anomalies such as ocular albinism, cataract, delayed neuropsychomotor development, sensorineural hearing loss, dolicocephaly, high arched palate, widely spaced teeth, anemia, and/or nystagmus.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Synonyms: Cross syndrome, Kramer Syndrome, Oculocerebral Hypopigmentation Syndrome of Preus, Oculocerebral syndrome with hypopigmentation
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