Literature DB >> 7669384

Adrenal 21-hydroxylase deficiency in childhood: 25 years' experience.

Y J Lim1, J A Batch, G L Warne.   

Abstract

OBJECTIVE: To review past and present management of congenital adrenal hyperplasia at a single centre, as a guide to best practice.
METHODOLOGY: The records of 89 patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency managed in a children's hospital in Australia over a period of 25 years were reviewed.
RESULTS: The diagnosis was made in infancy in 66 patients (37 males and 29 females) and later in 23 (11 males and 12 females). The mean age for genitoplasty in females with ambiguous genitalia was 18 months before 1984 and 3 months thereafter. Significant differences were found between males and females presenting after infancy with regard to virilization, bone age advancement, risk of true precocious puberty and final height. The mean final height standard deviation scores for seven males and seven females treated from infancy were -1.32 and -1.26, respectively.
CONCLUSIONS: The results emphasize the importance of early diagnosis and good control in ensuring a good outcome for patients with 21-hydroxylase deficiency.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7669384     DOI: 10.1111/j.1440-1754.1995.tb00790.x

Source DB:  PubMed          Journal:  J Paediatr Child Health        ISSN: 1034-4810            Impact factor:   1.954


  6 in total

1.  Final adult height in children with congenital adrenal hyperplasia treated with growth hormone.

Authors:  Karen Lin-Su; Madeleine D Harbison; Oksana Lekarev; Maria G Vogiatzi; Maria I New
Journal:  J Clin Endocrinol Metab       Date:  2011-03-30       Impact factor: 5.958

2.  Growth and reproductive outcomes in congenital adrenal hyperplasia.

Authors:  Todd D Nebesio; Erica A Eugster
Journal:  Int J Pediatr Endocrinol       Date:  2010-02-01

3.  Management of 21-hydroxylase deficiency congenital adrenal hyperplasia: A survey of Canadian paediatric endocrinologists.

Authors:  Robert Stein; Diane Wherrett; Denis Daneman
Journal:  Paediatr Child Health       Date:  2005-07       Impact factor: 2.253

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

Authors:  Helmuth G Dörr; Hartmut A Wollmann; Berthold P Hauffa; Joachim Woelfle
Journal:  BMC Endocr Disord       Date:  2018-06-08       Impact factor: 2.763

5.  Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: A five-year retrospective study in the Children's Hospital of Damascus, Syria.

Authors:  Lina Ibrahem Sheikh Alshabab; Assad AlebrahIm; Ahmad Kaddoura; Sahar Al-Fahoum
Journal:  Qatar Med J       Date:  2015-07-31

6.  Precocious Puberty in Boys: A Study Based on Five Years of Data from a Single Center in Northern China

Authors:  Liu Ziqin; Li Xiaohui; Chen Xiaobo
Journal:  J Clin Res Pediatr Endocrinol       Date:  2021-05-20
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.