Growth Pattern and Clinical Profile of Indian Children with Classical 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia on Treatment

Growth Pattern ◽

Clinical Profile ◽

Adrenal Hyperplasia ◽

Indian Children ◽

Hydroxylase Deficiency ◽

Growth Pattern during the First 36 Months of Life in Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency)

Hormone Research ◽

10.1159/000185361 ◽

1997 ◽

Vol 47 (1) ◽

pp. 17-22 ◽

Cited By ~ 5

Author(s):

Nicoletta Gasparini ◽

Salvatore Di Maio ◽

Mariacarolina Salerno ◽

Alessandro Argenziano ◽

Adriana Franzese ◽

...

Keyword(s):

Growth Pattern ◽

Adrenal Hyperplasia ◽

Hydroxylase Deficiency ◽

Molecular Characterization of Mutations in Indian Children with Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency

Journal of Pediatric Endocrinology and Metabolism ◽

10.1515/jpem.2001.14.1.27 ◽

2001 ◽

Vol 14 (1) ◽

Cited By ~ 11

Author(s):

R. Mathur ◽

P.S.N. Menon ◽

M. Kabra ◽

R.K. Goyal ◽

I.C. Verma

Keyword(s):

Molecular Characterization ◽

Adrenal Hyperplasia ◽

Indian Children ◽

Hydroxylase Deficiency ◽

Abstract #805: Male Infertility in Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Endocrine Practice ◽

10.1016/s1530-891x(20)43657-2 ◽

2005 ◽

Vol 11 ◽

pp. 4-5

Author(s):

Shanjian Zhu ◽

Harris C. Taylor ◽

Baha Arafah ◽

Thomas A. Murphy

Keyword(s):

Male Infertility ◽

Adrenal Hyperplasia ◽

Hydroxylase Deficiency ◽

Late diagnosis of classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Experimental and Clinical Endocrinology & Diabetes ◽

10.1055/s-2006-932899 ◽

2006 ◽

Vol 114 (S 1) ◽

Author(s):

K Müssig ◽

S Kaltenbach ◽

C Maser-Gluth ◽

MF Hartmann ◽

SA Wudy ◽

...

Keyword(s):

Late Diagnosis ◽

Adrenal Hyperplasia ◽

Hydroxylase Deficiency ◽

Classic Congenital Adrenal Hyperplasia ◽

The diagnosis of nonclassical congenital adrenal hyperplasia due to 21 hydroxylase deficiency in woman can be established by genetic testing or urine steroid profile analysis but not by ACTH stimulation test

Endocrine Abstracts ◽

10.1530/endoabs.32.p18 ◽

2013 ◽

Author(s):

Urszula Ambroziak ◽

Anna Kepczynska-Nyk ◽

Karolina Nowak ◽

Ewa Maria Malunowicz ◽

Emilia Morawska ◽

...

Keyword(s):

Genetic Testing ◽

Profile Analysis ◽

Adrenal Hyperplasia ◽

Acth Stimulation Test ◽

Acth Stimulation ◽

Hydroxylase Deficiency ◽

Steroid Profile ◽

21 Hydroxylase Deficiency ◽

Urine Steroid

Cardiovascular and metabolic risk factors in children and adolescents with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Endocrine Abstracts ◽

10.1530/endoabs.63.p880 ◽

2019 ◽

Author(s):

Silvia Paredes ◽

Marta Alves ◽

Fabia Carvalho ◽

Maria Miguel Gomes ◽

Sofia Martins ◽

...

Keyword(s):

Risk Factors ◽

Children And Adolescents ◽

Metabolic Risk Factors ◽

Metabolic Risk ◽

Adrenal Hyperplasia ◽

Hydroxylase Deficiency ◽

Adrenal morphology in a large cohort of adult subjects with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Endocrine Abstracts ◽

10.1530/endoabs.63.p60 ◽

2019 ◽

Author(s):

Claudia Oriolo ◽

Daniela Ibarra Gasparini ◽

Paola Altieri ◽

Francesca Ruffilli ◽

Francesca Corzani ◽

...

Keyword(s):

Large Cohort ◽

Adrenal Hyperplasia ◽

Hydroxylase Deficiency ◽

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an endocrine society clinical practice guideline

Yearbook of Paediatric Endocrinology ◽

10.1530/ey.16.8.5 ◽

2019 ◽

Author(s):

Speiser PW ◽

Arlt W ◽

Auchus RJ ◽

Baskin LS ◽

Conway GS ◽

...

Keyword(s):

Clinical Practice ◽

Clinical Practice Guideline ◽

Practice Guideline ◽

Adrenal Hyperplasia ◽

Hydroxylase Deficiency ◽

Endocrine Society ◽

Congenital adrenal hyperplasia in children due to 21-hydroxylase deficiency: clinical features, complications and approaches to their correction

SOVREMENNAYA PEDIATRIYA ◽

10.15574/sp.2015.68.123 ◽

2015 ◽

pp. 123-127

Author(s):

N. Zelinska ◽

◽

N. Pogadaeva ◽

E. Globa ◽

I. Shevchenko ◽

...

Keyword(s):

Clinical Features ◽

Adrenal Hyperplasia ◽

Hydroxylase Deficiency ◽

Faculty Opinions recommendation of Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family members.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1162755.624351 ◽

2009 ◽

Author(s):

Robert Dluhy ◽

Florencia Halperin

Keyword(s):

Molecular Characterization ◽

Family Members ◽

Adrenal Hyperplasia ◽

Hydroxylase Deficiency ◽