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Article

[Leydig cell hypoplasia(agenesis)].

Nihon rinsho. Japanese journal of clinical medicine - 1 Feb 2004

Koyama Satomi, Arisaka Osamu

Abstract excerpt

Leydig cell hypoplasia(LCH) or agenesis, which has an autosomal recessive inheritance pattern, is a well defined form of male pseudohermaphroditism resulting from inadequate fetal testicular Leydig cell differentiation. These patients exhibit a wide clinical spectrum that ranges from phenotypic f...

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Identifiers

PMID: 14968545

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-14968545-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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[Leydig cell hypoplasia(agenesis)].PMID 14968545Read ↗

[Leydig cell hypoplasia (Leydig cell aplasia)].Semantic proximity Read ↗

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[Inactivating and activating mutations of the human LH/hCG receptor leading to male pseudohermaphroditism and familial male-limited precocious puberty].Semantic proximity Read ↗

[Congenital hypogonadotropic hypogonadism].Semantic proximity Read ↗

Male Hypogonadism and Disorders of Sex DevelopmentSemantic proximity Read ↗

Origin, Development and Regulation of Human Leydig CellsSemantic proximity Read ↗

[Genetic aspects of fertility disorders].Semantic proximity Read ↗

Inactivating mutations of the human luteinizing hormone receptor in both sexes.Semantic proximity Read ↗

Fetal Leydig cells: What we know and what we don'tSemantic proximity Read ↗

Luteinizing hormone receptor mutations in disorders of sexual development and cancer.Semantic proximity Read ↗

Reproductive Phenotypes in Men With Acquired or Congenital Hypogonadotropic Hypogonadism: A Comparative Study.Semantic proximity Read ↗

Mutations in a novel, cryptic exon of the luteinizing hormone/chorionic gonadotropin receptor gene cause male pseudohermaphroditism.Semantic proximity Read ↗

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