In Sweden, a baby girl developed masculinized genital changes after skin contact with her father using testosterone gel, ...

The lack of form from Hendrick Motorsports driver Kyle Larson is put on full display following yet another disappointing ...

Kallmann syndrome is an inherited condition, and several genes are linked to the syndrome. These are found on different chromosomes and have a different inheritance pattern. The genetic cause of the ...

Mutations in the KAL-1 gene localized at Xp22.3 have been shown to be responsible for the X-linked Kallmann syndrome (KS), a disorder characterized by the association of hypogonadotropic hypogonadism ...

She had hoped to study children directly, but the most intense medical interventions related to the syndrome are concentrated in the first years of life.

This report details a case of a female patient with genetically confirmed Kallmann syndrome, which was found to be related to a novel molecular variant of the FGFR1 gene. We present a case of a ...

With accurate diagnosis, personalised treatment, and proper medical guidance, many men with genetic infertility can achieve fatherhood and experience the joy of parenthood.

Kallmann syndrome causes hypogonadotropic hypogonadism, a condition where the ovaries or testes do not produce enough sex hormones. It also causes an impaired sense of smell. The syndrome is present ...

ABSTRACT: Topic: Kallmann syndrome (KS) is a congenital olfacto-genital disease. Affected persons show an absence of physical pubertal development, and their sense of smell is reduced or absent ...

Background: Kallmann syndrome (KS) is a rare developmental disorder. Our previous metabolomics work showed substantial changes in linoleic acid and glycerophospholipid metabolism in KS. Here, we ...