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




homoit0002863
Leydig cell hypoplasia
Engelska
LCH
Engelska
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.
Engelska
Developed during an extended collaboration with interACT: Advocates for Intersex Youth, 2022-2023.
Engelska
2023-06-28 18:13:33 UTC
2025-02-23 07:12:57 UTC

Hierarkisk vy

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


Andra format (inklusive språkidentifierare): N-Triples, JSON-LD, Extended JSON, TTL, XML, MARC XML


Äldre format (utan språkidentifierare) N-Triples, JSON-LD, TTL