Rare and severe complications of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: 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: Rare and severe complications of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a case report ; volume:7 ; number:1 ; day:6 ; month:2 ; year:2013 ; pages:1-6 ; date:12.2013
Journal of medical case reports ; 7, Heft 1 (6.2.2013), 1-6, 12.2013

Creator: Ferreira, Florbela

Contributor: Martins, João Martin
do Vale, Sónia
Esteves, Rui
Nunes, Garção
Carmo, Isabel do
SpringerLink (Online service)

DOI: 10.1186/1752-1947-7-39

URN: urn:nbn:de:1111-20160711645

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:46 AM CEST

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Ferreira, Florbela
Martins, João Martin
do Vale, Sónia
Esteves, Rui
Nunes, Garção
Carmo, Isabel do
SpringerLink (Online service)

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Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany

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Novel therapeutic approaches for Congenital Adrenal Hyperplasia

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Congenital adrenal hyperplasia

Growth in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Novel treatments for congenital adrenal hyperplasia

Ethnic disparity in 21-hydroxylase gene mutations identified in Pakistani congenital adrenal hyperplasia patients

Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia

Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany

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Rare and severe complications of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a case report

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Other Objects (12)

Congenital adrenal hyperplasia

Growth in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Novel treatments for congenital adrenal hyperplasia

Ethnic disparity in 21-hydroxylase gene mutations identified in Pakistani congenital adrenal hyperplasia patients

Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia

Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany

Adrenarche and Puberty in Children with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany

Novel therapeutic approaches for Congenital Adrenal Hyperplasia

Congenital lipoid adrenal hyperplasia in twin sisters

Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency

Congenital adrenal hyperplasia

Growth in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Novel treatments for congenital adrenal hyperplasia

Ethnic disparity in 21-hydroxylase gene mutations identified in Pakistani congenital adrenal hyperplasia patients

Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia

Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany

Adrenarche and Puberty in Children with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany

Novel therapeutic approaches for Congenital Adrenal Hyperplasia

Congenital lipoid adrenal hyperplasia in twin sisters

Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency

Congenital adrenal hyperplasia

Growth in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Novel treatments for congenital adrenal hyperplasia

Ethnic disparity in 21-hydroxylase gene mutations identified in Pakistani congenital adrenal hyperplasia patients

Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia

Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany

Adrenarche and Puberty in Children with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany

Novel therapeutic approaches for Congenital Adrenal Hyperplasia

Congenital lipoid adrenal hyperplasia in twin sisters

Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency

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