Olfactory Phenotypic Spectrum in Idiopathic Hypogonadotropic Hypogonadism: Pathophysiological and Genetic Implications | Zendy

Hilana Lewkowitz-Shpuntoff | Zendy; Virginia Hughes | Zendy; Lacey Plummer | Zendy; Margaret Au | Zendy; Richard L. Doty | Zendy; Stephanie B. Seminara | Zendy; Yee-Ming Chan | Zendy; Nelly Pitteloud | Zendy; William F. Crowley | Zendy; Ravikumar Balasubramanian | Zendy

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Olfactory Phenotypic Spectrum in Idiopathic Hypogonadotropic Hypogonadism: Pathophysiological and Genetic Implications

Author(s) -

Hilana Lewkowitz-Shpuntoff,

Virginia Hughes,

Lacey Plummer,

Margaret Au,

Richard L. Doty,

Stephanie B. Seminara,

Yee-Ming Chan,

Nelly Pitteloud,

William F. Crowley,

Ravikumar Balasubramanian

Publication year - 2011

Publication title -

the journal of clinical endocrinology and metabolism

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 2.206

H-Index - 353

eISSN - 1945-7197

pISSN - 0021-972X

DOI - 10.1210/jc.2011-2041

Subject(s) - hyposmia , kallmann syndrome , anosmia , hypogonadotropic hypogonadism , olfactory system , medicine , pathophysiology , olfaction , endocrinology , biology , neuroscience , disease , psychiatry , covid-19 , hormone , infectious disease (medical specialty)

The olfactory phenotype in patients with idiopathic hypogonadotropic hypogonadism (IHH) ranges from complete anosmia (Kallmann syndrome) to normosmia (normosmic IHH). However, the true prevalence of intermediary olfactory phenotypes (hyposmia) in IHH patients has not yet been assessed, and systematic correlations with anatomical and genetic abnormalities have not been reported.

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