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Crandall syndrome

Orpha number ORPHA202
Synonym(s) Alopecia - deafness - hypogonadism
Prevalence Unknown
Inheritance
  • Autosomal recessive
Age of onset No data available
ICD-10 -
OMIM -
UMLS
  • C0432348
MeSH -
MedDRA -
SNOMED CT
  • 278098005

Summary

This 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.


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