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Paraplegia - intellectual deficit - hyperkeratosis

Orpha number ORPHA2824
Prevalence of rare diseases <1 / 1 000 000
Inheritance
  • X-linked recessive
Age of onset No data available
ICD 10 code
  • F79.1
  • G82.1
MIM number
Synonym(s) Fitzsimmons-McLachlan-Gilbert syndrome

Summary

This syndrome is characterized by intellectual deficit, spasticity in the lower limbs (spastic paraplegia), pes cavus deformity of both feet, an abnormal gait, and palmar and plantar hyperkeratosis. It has been reported in four brothers. The mother of the affected boys had normal intelligence, plantar hyperkeratosis and a strong facial resemblance to her retarded sons. Her three daughters were normal. This syndrome most likely an X-linked recessive condition. *Author: Orphanet (February 2006)*.

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