Exploring the Genetic Diversity of Isolated Hypogonadotropic Hypogonadism and Its Phenotypic Spectrum: A Case Series

BACKGROUND: Isolated hypogonadotropic hypogonadism (IHH) is a rare disorder being classified as Kallmann syndrome (KS). The present study was conducted to study the genotype and relative proportion of different genetic mutations in IHH and to assess its correlation with phenotype. METHODS: Eleven co...

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Detalles Bibliográficos
Autores principales: Danda, Vijay Sheker Reddy, Paidipelly, Srinivas Rao, Verepula, Madhavi, Lodha, Piyush, Thaduri, Krishna Reddy, Konda, Chaitanya, Ruhi, Apsia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Avicenna Research Institute 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7903671/
https://www.ncbi.nlm.nih.gov/pubmed/33680884
http://dx.doi.org/10.18502/jri.v22i1.4994

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7903671/
https://www.ncbi.nlm.nih.gov/pubmed/33680884
http://dx.doi.org/10.18502/jri.v22i1.4994

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