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Leydig cell hypoplasia, type II

MedGen UID:
392934
•Concept ID:
C2673497
•
Disease or Syndrome
Synonym: Leydig cell hypoplasia, partial
 
OMIM®: 152790; 238320

Professional guidelines

PubMed

The undescended testis: diagnosis, treatment and long-term consequences.
Mathers MJ, Sperling H, Rübben H, Roth S
Dtsch Arztebl Int 2009 Aug;106(33):527-32. Epub 2009 Aug 14 doi: 10.3238/arztebl.2009.0527. PMID: 19738919Free PMC Article
Inactivating mutations of LH and FSH receptors--from genotype to phenotype.
Latronico AC, Arnhold IJ
Pediatr Endocrinol Rev 2006 Sep;4(1):28-31. PMID: 17021580
Testicular histology following chronic gonadotropin-releasing hormone agonist treatment.
Rajfer J, Swerdloff RS, Heber DM
Fertil Steril 1984 Nov;42(5):765-71. doi: 10.1016/s0015-0282(16)48205-1. PMID: 6436070

Recent clinical studies

Diagnosis

Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type II.
Hassan HA, Mazen I, Elaidy A, Kamel AK, Eissa NR, Essawi ML
Hormones (Athens) 2024 Jun;23(2):305-312. Epub 2024 Mar 25 doi: 10.1007/s42000-024-00546-x. PMID: 38526829Free PMC Article

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    Related information

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      Clinical tests in GTR
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