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Crandall syndrome
rareThis syndrome is characterized by progressive sensorineural deafness, alopecia and hypogonadism with LH and GH deficiencies. It has been described in three brothers. It resembles Bjrnstad's syndrome that combines irregular pili torti and deafness. It is probably inherited as and autosomal recessive disorder.
- Identifiers
- MONDO:0016067 Orphanet:202
- Part of
- Syndromic disease
- Also known as
- alopecia deafness hypogonadism · alopecia-deafness-hypogonadism syndrome · alopecia-sensorineural deafness-hypogonadism syndrome
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