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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Detaylı Bibliyografya
Yayımlandı:J Reprod Infertil
Asıl Yazarlar: Danda, Vijay Sheker Reddy, Paidipelly, Srinivas Rao, Verepula, Madhavi, Lodha, Piyush, Thaduri, Krishna Reddy, Konda, Chaitanya, Ruhi, Apsia
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Avicenna Research Institute 2021
Konular:
Original Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7903671/
https://ncbi.nlm.nih.gov/pubmed/33680884
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18502/jri.v22i1.4994
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