x

Search for a rare disease

* (*) mandatory field

Other search option(s)

Suggest an update

(*) Required fields.

Attention

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed.

Captcha image

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

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.