Familial glucocorticoid deficiency presenting with hyperpigmentation, gigantism, and motor development delay: a case report

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1752-1947

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Familial glucocorticoid deficiency presenting with hyperpigmentation, gigantism, and motor development delay: a case report ; volume:13 ; number:1 ; day:4 ; month:9 ; year:2019 ; pages:1-4 ; date:12.2019
Journal of medical case reports ; 13, Heft 1 (4.9.2019), 1-4, 12.2019

Creator: Uyangoda, Kanchana
Kamalanathan, Phirarthana
Mettananda, Sachith

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13256-019-2206-5

URN: urn:nbn:de:101:1-2020010919531036538223

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:50 AM CEST

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Uyangoda, Kanchana
Kamalanathan, Phirarthana
Mettananda, Sachith
SpringerLink (Online service)

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Familial glucocorticoid deficiency presenting with hyperpigmentation, gigantism, and motor development delay: a case report

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Other Objects (12)

Familial glucocorticoid deficiency presenting with generalized hyperpigmentation in an Egyptian child: a case report

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ADCY5-related dyskinesia presenting as familial myoclonus-dystonia

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ADCY5-related dyskinesia presenting as familial myoclonus-dystonia

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Familial Glucocorticoid Deficiency Type 1 due to a Novel Compound Heterozygous MC2R Mutation

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ADCY5-related dyskinesia presenting as familial myoclonus-dystonia

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