| Literature DB >> 27502037 |
Samuel D Quaynor1, Maggie E Bosley2, Christina G Duckworth2, Kelsey R Porter2, Soo-Hyun Kim3, Hyung-Goo Kim4, Lynn P Chorich4, Megan E Sullivan4, Jeong-Hyeon Choi5, Richard S Cameron6, Lawrence C Layman7.
Abstract
The genetic basis is unknown for ∼60% of normosmic hypogonadotropic hypogonadism (nHH)/Kallmann syndrome (KS). DNAs from (17 male and 31 female) nHH/KS patients were analyzed by targeted next generation sequencing (NGS) of 261 genes involved in hypothalamic, pituitary, and/or olfactory pathways, or suggested by chromosome rearrangements. Selected variants were subjected to Sanger DNA sequencing, the gold standard. The frequency of Sanger-confirmed variants was determined using the ExAC database. Variants were classified as likely pathogenic (frameshift, nonsense, and splice site) or predicted pathogenic (nonsynonymous missense). Two novel FGFR1 mutations were identified, as were 18 new candidate genes including: AMN1, CCKBR, CRY1, CXCR4, FGF13, GAP43, GLI3, JAG1, NOS1, MASTL, NOTCH1, NRP2, PALM2, PDE3A, PLEKHA5, RD3, and TRAPPC9, and TSPAN11. Digenic and trigenic variants were found in 8/48 (16.7%) and 1/48 (2.1%) patients, respectively. NGS with confirmation by Sanger sequencing resulted in the identification of new causative FGFR1 gene mutations and suggested 18 new candidate genes in nHH/KS.Entities:
Keywords: Delayed puberty; GnRH deficiency; Hypogonadotropic hypogonadism; Kallmann syndrome; Next generation DNA sequencing
Mesh:
Year: 2016 PMID: 27502037 DOI: 10.1016/j.mce.2016.08.007
Source DB: PubMed Journal: Mol Cell Endocrinol ISSN: 0303-7207 Impact factor: 4.102