Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome

Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome is characterized by ichthyosis, hepatosplenomegaly and late-onset cerebellar ataxia. It has been described in two brothers. Transmission is either autosomal recessive or X-linked.

Also known as: Dykes-Markes-Harper syndrome, Dykes-Marks-Harper syndrome, Dykes Markes Harper syndrome, ichthyosis, hepatosplenomegaly, and cerebellar degeneration

0 clinical trials for this condition and its sub-types, 0 tagged with Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome itself.