Results 171 to 180 of about 2,952 (186)

Kallmann's syndrome and mental handicap

Journal of Intellectual Disability Research, 1992
ABSTRACT. A case of Kallmann's syndrome is reported in a 62‐year‐oId mentally handicapped man with clinical and laboratory characteristics of the syndrome. The literature is reviewed and the possible associations with mental handicap explored.
M. G. A. Izmeth, J. C. Rigby, H. Obaydi
openaire   +3 more sources

Kallmann Syndrome.

1995
7th ...
BALLABIO, ANDREA, ZOGHBI H. Y.
openaire   +2 more sources

Das Kallmann-Syndrom

Reproduktionsmedizin, 2003
Zusammenfassung Das Kallmann-Syndrom ist mit einer Inzidenz von 1:7500 beim Mann eine der haufigsten Formen des Hypogonadismus. Bei Frauen tritt die Erkrankung deutlich seltener auf (Verhaltnis Mann/Frau =7:1). Es handelt sich um eine genetische Erkrankung mit den Hauptsymptomen Hypogonadismus und Riechstorung – bis hin zur Anosmie.
C. Keck, D. Denschlag
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Kallmann’s Syndrome with Diabetes Insipidus

Endocrine Practice, 1995
A case is presented of a male with Kallmann's syndrome who at the age of 27 developed central diabetes insipidus. Previously, Kallmann's syndrome has been found to be associated with an altered osmotic threshold for vasopressin release and impaired thirst sensation, but to our knowledge, this is the first reported association with diabetes insipidus.
Kenneth B. Horwitz, Barry Z. Izenstein
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Treatment of Kallmann Syndrome

JAMA: The Journal of the American Medical Association, 1976
To the Editor.— I would like to share with your readers a fairly common case in which the unhappy outcome might have been averted with proper planning. Report of a Case.— A 27-year-old man was seen at another hospital for cellulitis. He was a prepubertal male as confirmed by history and physical examination.
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Kallmann syndrome: Diagnostics and management

Clinica Chimica Acta
Kallmann syndrome is a genetic disorder characterized by delayed or absence of puberty and a reduced or absent sense of smell (anosmia). Kallmann syndrome is a form of hypogonadotropic hypogonadism due to lack of the production of sex hormones which is associated with development of secondary sexual characteristics.
Rajiv Kumar Yadav, Baiyu Qi, Jianping Wen, Xiaokun Gang, Santasree Banerjee   +4 more
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Kallmann syndrome: towards molecular pathogenesis

Molecular and Cellular Endocrinology, 2001
Gonadotropin Releasing Hormone (GnRH) is a key regulator of reproduction and sexual behaviour. During the last decade, embryological studies have clarified the question of the early development of GnRH-synthesising neurones before the onset of neurosecretion.
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Kallmann's Syndrome

Practica Oto-Rhino-Laryngologica, 1976
Takeo Sato, Isao Miyakawa, Masahide Munemura, Kousuke Aoki   +3 more
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Kallmann Syndrome

2000
Hardelin, Jean-Pierre, Soussi-Yanicostas, Nadia, Ardouin, O., Levilliers, Jacqueline, Petit, Christine   +4 more
openaire   +3 more sources

Das Kallmann-Syndrom [PDF]

Zeitschrift für Sexualforschung, 2010
Johannes Hofmann, Hertha Richter-Appelt
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