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Abdallat Davis Farrage syndrome
Classification and external resources |
| OMIM |
270750 |
Abdallat Davis Farrage syndrome is a phakomatosis consisting of disordered skin and hair pigmentation, progressive spastic paraparesis and peripheral neuropathy. It is also known as neurocutaneous syndrome, Abdallat type.
The syndrome is thought to be inherited as an autosomal recessive genetic trait.
Abdallat Davis Farrage syndrome has an autosomal recessive pattern of
inheritance.
[edit] Symptoms
[edit] References
- Abdallat A, Davis SM, Farrage J, McDonald WI (1980). "Disordered pigmentation, spastic paraparesis and peripheral neuropathy in three siblings: a new neurocutaneous syndrome". J Neurol Neurosurg Psychiatry 43 (11): 962–6. PMID 7441281
[edit] External links
