Síndrome de Kallmann (https://es.homosaurus.org/v3/homoit0002862)




Identificador
homoit0002862
Etiqueta preferida
Kallmann syndrome
Ingles
Etiqueta alternativa
Hypogonadotropic hypogonadism
Ingles
Descripción
Kallmann syndrome can occur in people with XX or XY chromosomes and is a form of hypogonadism. People with Kallmann syndrome and XY chromosomes are often born with a smaller-than-typical penis and undescended testes. In adolescence, most people with Kallmann syndrome will either start puberty later than usual or not experience typical pubertal changes (such as developing facial hair and a deeper voice for people with XY chromosomes or developing breasts and starting to menstruate for people with XX chromosomes) unless they receive hormone therapy. Kallmann syndrome also affects someone’s sense of smell.
Ingles
Colaboradores
Developed during an extended collaboration with interACT: Advocates for Intersex Youth, 2022-2023.
Ingles
Emitido (creado)
2023-06-28 18:12:04 UTC
Modificado
2025-02-23 07:12:57 UTC
Más amplio
Variaciones intersex [homoit0000669]

Visualización de jerarquía

Variaciones intersex
Síndrome de Kallmann


Otros formatos (incluidos identificadores de idioma): N-Triples, JSON-LD, Extended JSON, TTL, XML, MARC XML


Formatos heredados (sin identificadores de idioma) N-Triples, JSON-LD, TTL

Homosaurus.org es un servicio de datos vinculado mantenido por el Digital Transgender Archive
Este vocabulario está disponible bajo una licencia Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 internacional (CC BY NC-ND 4.0)