Hereditary sensory and autonomic neuropathy type 7

Disease Export to PDF
Name:
Hereditary sensory and autonomic neuropathy type 7
Description:
A rare, genetic, periphery neuropathy characterized by a congenital insensitivity to pain, muscular hypotonia and gastrointestinal disturbances. Patients present with delayed motor milestones achievement, self-mutilations, skin ulcers, poor wound healing, painless fractures, hyperhidrosis, abdominal discomfort, diarrhea and/or constipation. Cognitive development is normal.
ORPHAcode:
391397
Synonyms:
CIP with hyperhidrosis and gastrointestinal dysfunction
Congenital insensitivity to pain with hyperhidrosis and gastrointestinal dysfunction
HSAN with hyperhidrosis and gastrointestinal dysfunction
HSAN7
Hereditary sensory and autonomic neuropathy type VII
Hereditary sensory and autonomic neuropathy with hyperhidrosis and gastrointestinal dysfunction
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Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14