File:Leydig cells stained for LHCGR1.jpg
Leydig_cells_stained_for_LHCGR1.jpg (404 × 322 pixels, file size: 16 KB, MIME type: image/jpeg)
Leydig Cells
Labelled for luteinizing hormone/chorionic gonadotropin receptor (LHCGR).
Mutation in this receptor can cause Leydig cell hypoplasia (LCH).
Leydig cell hypoplasia, (LCH) is an autosomal recessive disorder in individuals with a 46,XY karyotype who have a predominantly female phenotype (blind-ending vagina, absence of breast development, primary amenorrhea, presence of testicular structures) that is with gonads of one sex, external genitalia of opposite. One cause has been recently identified as the presence of a cryptic exon in the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) gene.
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Yi efo/eka'e gwa ebo wo le nyangagi wuncin ye kamina wunga tinya nan
| Gwalagizhi | Nyangagi | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 11:46, 13 May 2010 | | 404 × 322 (16 KB) | S8600021 (talk | contribs) | ==Leydig Cells== Labelled for luteinizing hormone/chorionic gonadotropin receptor (LHCGR). Mutation in this receptor can cause Leydig cell hypoplasia (LCH). Leydig cell hypoplasia, (LCH) is an autosomal recessive disorder in individuals with a 46,XY ka |
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