Atypical Presentation of A Patient With Both Kallmann Syndrome and A Craniopharyngioma: Case Report and Literature Review

Author:

Jonklaas Jacqueline

Publisher

Elsevier BV

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

Reference42 articles.

1. Kallmann syndrome: from genetics to neurobiology;Rugarli;JAMA.,1993

2. A gene deleted in Kallmann’s syndrome shares homology with neural cell adhesion and axonal path-finding molecules;Franco;Nature.,1991

3. The genetic and clinical heterogeneity of gonadotropin-releas-ing hormone deficiency in the human;Waldstreicher;J Clin Endocrinol Metab.,1996

4. Male hypogonadotropic hypogonadism;Whitcomb;Endocrinol Metab Clin North Am.,1993

5. Clinical counterpoint: gonadotropin-releasing hormone deficiency; perspectives from clinical investigation;Crowley;Endocr Rev.,1992

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1. Case Report: Multiple prolactinomas in a young man with Kallmann syndrome and familial hypocalciuric hypercalcemia;Frontiers in Endocrinology;2023-10-30

2. Genetics of Arachnoid Cysts;Arachnoid Cysts;2023

3. Hypothalamic Obesity and Wasting Syndromes;The Human Hypothalamus;2020-12-25

4. Disorders of Hypothalamo‐Pituitary Axis;Brook's Clinical Pediatric Endocrinology;2019-08-30

5. A case of Kallmann syndrome associated with a non-functional pituitary microadenoma;Endocrinology, Diabetes & Metabolism Case Reports;2018-04-17

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