Leydig cell hypoplasia (https://homosaurus.org/v3/homoit0002863)




Identifiant
homoit0002863
Étiquette privilégiée
Leydig cell hypoplasia
English
Étiquette alternative
LCH
English
Description
People with Leydig cell hypoplasia (LCH) have XY chromosomes and a genetic insensitivity to luteinizing hormone. LCH can be either complete (known as LCH Type 1) or partial (known as LCH Type 2). Luteinizing hormone is typically responsible for the development of Leydig cells in the testicles and for signaling for those cells to produce androgens like testosterone. Someone with LCH will develop few or no Leydig cells and therefore will produce less testosterone than is typical.
English
Contributeurs
Developed during an extended collaboration with interACT: Advocates for Intersex Youth, 2022-2023.
English
Issued (Created)
2023-06-28 18:13:33 UTC
Modified
2023-06-28 18:13:33 UTC
Plus large
Intersex variations [homoit0000669]
Plus précis
Type 1 Leydig cell hypoplasia [homoit0002879]
Type 2 Leydig cell hypoplasia [homoit0002881]

Affichage de la hiérarchie

Intersex variations
Leydig cell hypoplasia
Type 1 Leydig cell hypoplasia
Type 2 Leydig cell hypoplasia


Autres formats (y compris les identifiants de langue): N-Triples, JSON-LD, Extended JSON, TTL, XML, MARC XML


Formats hérités (sans identifiants de langue) N-Triples, JSON-LD, TTL

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