Results 151 to 160 of about 2,952 (186)

Chromosome Xp22.3 deletion syndrome with X-linked ichthyosis, Kallmann syndrome, short stature, generalized epilepsy, hearing loss, attention deficit hyperactivity disorder, and intellectual disability – A rare report with review of literature

open access: gold
Pradeep Kumar Gunasekaran   +10 more
openalex   +1 more source

Kallmann Syndrome: A Late Diagnosis

open access: hybrid
Ricardo Pereira   +5 more
openalex   +2 more sources

Prevalence of pathogenic variants and digenic disease in patients diagnosed with normosmic hypogonadotropic hypogonadism/Kallmann Syndrome

open access: bronze
Alexandra M. Poch   +7 more
openalex   +2 more sources

Spontaneous Reversal of Kallmann Syndrome in a Patient with PCSK1 and HS6ST1 Mutations: A Case Report

open access: bronze
Alanna Asgeirsson   +10 more
openalex   +1 more source

Kallmann-Syndrom

Der Hautarzt, 2011
The Kallmann syndrome is a very rare congenital association of gonadotropin-releasing hormone deficiency and hyposmia or anosmia. Clinically it is characterized by low serum concentrations of testosterone and inadequate low levels of luteinizing hormone and follicle-stimulating hormone as well as incomplete sexual maturation, lack of secondary sexual ...
N.J. Neumann   +3 more
openaire   +3 more sources

Kallmann’s syndrome

The Indian Journal of Pediatrics, 2007
Kallmann's syndrome is a rare genetic disorder due to abnormal migration of olfactory axons and gonadotropin releasing hormone producing neurons, characterized by hypogonadism and anosmia. The prevalence of Kallmann's syndrome is 1:10,000 to 1:60,000 with a male to female ratio of 5:1.
Akhil M. Kulkarni   +4 more
openaire   +3 more sources

Kallmann's Syndrome and Transsexualism

Archives of Sexual Behavior, 2001
Until the present, in the world literature only one patient with Kallmann's syndrome has been reported who became transsexual. This patient was seen almost 50 years ago. In this report, a second case is presented to encourage studies of the sexual and gender identity development in these patients.
Bernd Meyenburg, Volkmar Sigusch
openaire   +3 more sources

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