Chromosomal Translocation t(13;16) in a Patient with Idiopathic Hypogonadotropic Hypogonadism

Autor:	Masashi Seita, Akira Ueda, Ikuo Kikuchi, Motohisa Nagamine, Kenroh Mihara, Masaru Minoda
Rok vydání:	1993
Předmět:	Adult Male congenital hereditary and neonatal diseases and abnormalities medicine.medical_specialty Kallmann syndrome Gonadotropin releasing hormone deficiency Chromosome Disorders Chromosomal translocation Translocation Genetic Gonadotropin-Releasing Hormone Erectile Dysfunction Testosterone deficiency Hypogonadotropic hypogonadism Internal medicine Internal Medicine Humans Medicine Ejaculation Testosterone Chromosome Aberrations Chromosomes Human Pair 13 business.industry Hypogonadism Chromosome Kallmann Syndrome General Medicine Luteinizing Hormone medicine.disease Pedigree Luteinizing Hormone Deficiency Endocrinology Follicle Stimulating Hormone business Genomic imprinting Pituitary Hormone-Releasing Hormones Chromosomes Human Pair 16
Zdroj:	Internal Medicine. 32:465-467
ISSN:	1349-7235 0918-2918
Popis:	A patient with idiopathic hypogonadotropic hypogonadism (IHH) had an apparently balanced reciprocal translocation involving chromosomes 13 and 16 [t(13;16)(q14.11;q24)]. The patient's father has the same chromosomal translocation with no apparent physical abnormalities. The role of the chromosomal translocation in this patient is discussed.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f5b97c827b616bcfa7f10131887c2f6 https://doi.org/10.2169/internalmedicine.32.465 Zobrazit plný text záznamu