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Kallmann Syndrome

Known as: kallman's syndrome, HHA, kallmans syndrome 
A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital… 
National Institutes of Health

Related topics

Related topics

22 relations
ACTH Deficiency, IsolatedANOS1 geneAnosmiaFGFR1 gene

Broader (4)

Congenital DisordersHypogonadismOlfaction DisordersSyndrome

Narrower (4)

Kallmann Syndrome 1Kallmann Syndrome 2 (disorder)Kallmann Syndrome 2 with Bimanual SynkinesiaKallmann syndrome, type 3, recessive

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2009
Review
2009
Hypogonadotropic Hypogonadism in Men with Type 2 Diabetes
Abstract It has recently been demonstrated that ≥ one-third of men with type 2 diabetes mellitus have low testosterone… 
Review
2007
Review
2007
Chronic rhinosinusitis patterns of illness.
Chronic rhinosinusitis is a complex, multifactorial illness that has genetic, infectious, immune, anatomic, allergic, and… 
Highly Cited
2006
Highly Cited
2006
Brain Perfusion Single Photon Emission Computed Tomography Findings in Patients with Posttraumatic Anosmia and Comparison with Radiological Imaging
Background Different techniques in neuroimaging have been proposed for assessment of olfactory dysfunction but they are not… 
Highly Cited
1996
Highly Cited
1996
Truncation at the C-terminus of the DAX-1 protein impairs its biological actions in patients with X-linked adrenal hypoplasia congenita.
The DAX-1 [DSS (dosage-sensitive sex)-AHC critical region in the X, gene 1] gene has been reported to be responsible for X-linked… 
Highly Cited
1994
Highly Cited
1994
Expression of the Kallmann syndrome gene in human fetal brain and in the manipulated chick embryo.
Kallmann syndrome is an inherited disorder characterized by an abnormality in olfactory system development. The gene for the X… 
Highly Cited
1990
Highly Cited
1990
Two families of low-copy-number repeats are interspersed on Xp22.3: implications for the high frequency of deletions in this region.
Review
1987
Review
1987
Neuropathology of “Septo‐optic Dysplasia” (de Morsier Syndrome) with Immunohistochemical Studies of the Hypothalamus and Pituitary Gland
The de Morsier syndrome, or septo-optic dysplasia, is a developmental anomaly characterized by involvement of the optic system… 
Highly Cited
1973
Highly Cited
1973
Hypogonadotropic eunuchoidism. I. Clinical study of the mode of inheritance.
Hypogonadotropic eunuchoidism is a well recognized form of familial hypogonadism characterized by selective gonadotropin… 
Highly Cited
1968
Highly Cited
1968
Familial hypogonadotropic hypogonadism with anosmia.
Hypogonadotropic hypogonadism with anosmia has been found in two brothers and a half sister, who are related through the same… 
Highly Cited
1959
Highly Cited
1959
THE USE OF AN OBJECT SORTING TEST IN ELUCIDATING THE HEREDITARY FACTOR IN SCHIZOPHRENIA
Much evidence is now available as to the importance of the hereditary factor in the causation of schizophrenic psychoses. However… 
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