CEDNIK syndrome

Disease Export to PDF
Name:
CEDNIK syndrome
Description:
A rare, genetic, neurocutaneous disease characterized by severe developmental abnormalities of the nervous system and aberrant differentiation of the epidermis. Patients present with a unique constellation of clinical signs described with the acronym CEDNIK: CErebral Dysgenesis, Neuropathy, Ichthyosis, and palmoplantar Keratoderma.
ORPHAcode:
66631
Synonyms:
Cerebral dysgenesis-neuropathy-ichthyosis-palmoplantar keratoderma syndrome
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Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14