Search for a rare disease
Other search option(s)
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
- Synonym(s):
- Alopecia-deafness-hypogonadism syndrome
- Alopecia-sensorineural deafness-hypogonadism syndrome
- Prevalence: Unknown
- Inheritance: Autosomal recessive
- Age of onset: No data available
- ICD-10: -
- OMIM: -
- UMLS: C0432348
- MeSH: -
- GARD: 1561
- MedDRA: -
Additional information
Further information on this disease
Health care resources for this disease
Research activities on this disease
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.