Premium
Novel homozygous deletion of segmental KAL1 and entire STS cause Kallmann syndrome and X‐linked ichthyosis in a Chinese family
Author(s) -
Xu H.,
Li Z.,
Wang T.,
Wang S.,
Liu J.,
Wang D. W.
Publication year - 2015
Publication title -
andrologia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.633
H-Index - 59
eISSN - 1439-0272
pISSN - 0303-4569
DOI - 10.1111/and.12397
Subject(s) - hypogonadotrophic hypogonadism , kallmann syndrome , endocrinology , hypogonadotropic hypogonadism , medicine , anosmia , ichthyosis , testosterone (patch) , hormone , dermatology , disease , covid-19 , infectious disease (medical specialty)
Summary Kallmann syndrome (KS) is a genetically heterogeneous disease characterised by hypogonadotrophic hypogonadism in association with anosmia or hyposmia. This condition affects 1 in 10 000 men and 1 in 50 000 women. Defects in seventeen genes including KAL1 gene contribute to the molecular basis of KS. We report the clinical characteristics, molecular causes and treatment outcome of two Chinese brothers with KS and X‐linked ichthyosis. The phenotypes of the patients were characterised by bilateral cryptorchidism, unilateral renal agenesis in one patient but normal kidney development in another. The patients had low serum testosterone, follicle‐stimulating hormone and luteinising hormone levels and a blunt response to the gonadotrophin‐releasing hormone stimulation test. After human chorionic gonadotrophin treatment, the serum testosterone levels were normalized, and the pubic hair, penis length and testicular volumes were greatly improved in both of the patients. The two affected siblings had the same novel deletion at Xp22.3 including exons 9‐14 of KAL1 gene and entire STS gene. Our study broadens the mutation spectrum in the KAL1 gene associated with KS and facilitates the genetic diagnosis and counselling for KS.