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Crandall syndrome
Disease definition
Crandall syndrome is characterized by progressive sensorineural deafness, alopecia and hypogonadism with LH and GH deficiencies. It has been described in three brothers. It resembles Björnstad's syndrome (see this term) that combines irregular pili torti and deafness. It is probably inherited as and autosomal recessive disorder.
ORPHA:202
Classification level: Disorder- Synonym(s):
- Alopecia-deafness-hypogonadism syndrome
- Alopecia-hearing loss-hypogonadism syndrome
- Alopecia-sensorineural deafness-hypogonadism syndrome
- Alopecia-sensorineural hearing loss-hypogonadism syndrome
- Prevalence: Unknown
- Inheritance: Autosomal recessive
- Age of onset: No data available
- ICD-10: -
- OMIM: -
- UMLS: C0432348
- MeSH: -
- GARD: 1561
- MedDRA: -
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