Inducción puberal con gonadotropinas en un varón adulto con síndrome de Kallmann
Gil Boixa, José Vicente; Bodoque Cubas, Javier; Serra Soler, Guillermo.
Med. clín (Ed. impr.)
; 161(11): 503-504, dic. 2023. ilus
Artículo en Español | IBECS (España) | ID: ibc-228159
Documentos relacionados
Live birth in male de novo Kallmann syndrome after cross-generational genetic sequencing.
Novel rare variants in FGFR1 and clinical characteristics analysis in a series of congenital hypogonadotropic hypogonadism patients.
[Clinical diagnosis and treatment of male Kallmann syndrome].
Mechanisms of Central Hypogonadism.
A novel homozygous nonsense NDNF variant in Kallmann syndrome.
[Missense mutation of SPRY4 gene in Kallmann syndrome: a case report].
A rare case of a 34-year-old patient diagnosed late with Kallmann syndrome: case report.
Convergent biological pathways underlying the Kallmann syndrome-linked genes Hs6st1 and Fgfr1.
SIN3A Defects Associated with Syndromic Congenital Hypogonadotropic Hypogonadism: An Overlap with Witteveen-Kolk Syndrome.
Genetic spectrum of Kallmann syndrome: Single-center experience and systematic review.