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




Identifierare
homoit0002863
Föredragen benämning
Leydig cell hypoplasia
Engelska
Variant
LCH
Engelska
Beskrivning
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
Bidragsgivare
Developed during an extended collaboration with interACT: Advocates for Intersex Youth, 2022-2023.
Engelska
Utfärdad (skapad)
2023-06-28 18:13:33 UTC
Ändrad
2025-02-23 07:12:57 UTC
Bredare
Intersex variations [homoit0000669]
Smalare
Type 1 Leydig cell hypoplasia [homoit0002879]
Type 2 Leydig cell hypoplasia [homoit0002881]

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

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