Reference results for Kallmann_syndrome from Search.com.

Kallmann syndrome - Genetics Home Reference

ghr.nlm.nih.gov/condition/kallmann-syndrome

Kallmann syndrome is a condition characterized by delayed or absent puberty and an impaired sense of smell. This disorder is a form of hypogonadotropic ...

Kallmann Syndrome - WebMD

www.webmd.com/sexual-conditions/kallmann-syndrome

Important It is possible that the main title of the report Kallmann Syndrome is not the name you expected. Please check the synonyms listing to find the ...

Kallmann Syndrome and Idiopathic Hypogonadotropic ...

emedicine.medscape.com/article/122824

Classic Kallmann syndrome (KS) and idiopathic hypogonadotropic hypogonadism (IHH) are rare genetic conditions that encompass the spectrum of isolated ...

Kallmann syndrome - Wikipedia, the free encyclopedia

https://en.wikipedia.org/wiki/Kallmann_syndrome

Kallmann syndrome is a genetic condition where the primary symptom is a failure to start puberty or a failure to fully complete it. It occurs in both males and ...

Kallmann Syndrome Symptoms, Diagnosis, Treatments and ...

www.rightdiagnosis.com/k/kallmann_syndrome/intro.htm

Kallmann Syndrome: Introduction. Kallmann Syndrome: A rare inherited condition characterized by hypogonadism, eunuchoidism and impaired or absent sense of smell.

Kallmann syndrome: MRI findings - PubMed Central (PMC)

www.ncbi.nlm.nih.gov/pmc/articles/PMC3830283

Kallmann syndrome (KS) is a disease clinically characterized by the association of hypogonadotrophic hypogonadism and anosmia or hyposmia. It is a neuronal migration ...

Information About Kallmann Syndrome - About.com Health

rarediseases.about.com/od/rarediseasesk/a/kallmann.htm

Information about the rare inherited disorder Kallmann syndrome, including its symptoms, diagnosis and treatment options.

Kallmann syndrome | Disease | Overview | Genetic and Rare ...

https://rarediseases.info.nih.gov/gard/10771/kallmann-syndrome/...

A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Kallmann syndrome

Kallmann Syndrome | Cigna

www.cigna.com/healthwellness/hw/medical-topics/kallmann-syndrome...

Kallmann syndrome (KS) is a rare genetic disorder in humans that is defined by a delay/absence of signs of puberty along with an absent/impaired sense of smell. A ...

Kallmann Syndrome - NORD (National Organization for Rare ...

rarediseases.org/rare-diseases/kallmann-syndrome

The diagnosis of Kallmann syndrome is based on the clinical evidence of arrested sexual maturation or hypogonadism and ... National Organization for Rare Disorders, Inc.