Regarding the Consensus Statement on 21-Hydroxylase Deficiency from the Lawson Wilkins Pediatric Endocrine Society and The European Society for Paediatric Endocrinology
العنوان: | Regarding the Consensus Statement on 21-Hydroxylase Deficiency from the Lawson Wilkins Pediatric Endocrine Society and The European Society for Paediatric Endocrinology |
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المؤلفون: | Duncan T. Wilcox, Christopher Woodhouse, L.-M. Liao, Patrick G. Duffy, Richard Stanhope, Catherine L Minto, Peter Cuckow, Naomi S. Crouch, P.G. Ransley, Ieuan Hughes, Gerard S. Conway, Peter C. Hindmarsh, Mehul T. Dattani, Les Perry, Imran Mushtaq, John Achermann, Sarah M. Creighton, Angela Barnicoat, Caroline Brain |
المصدر: | The Journal of Clinical Endocrinology & Metabolism. 88:3455-3455 |
بيانات النشر: | The Endocrine Society, 2003. |
سنة النشر: | 2003 |
مصطلحات موضوعية: | Male, medicine.medical_specialty, Consensus, Statement (logic), Pediatric endocrinology, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Population, Pediatrics, Biochemistry, Endocrinology, Internal medicine, medicine, Humans, Endocrine system, Congenital adrenal hyperplasia, Genitalia, Child, education, Societies, Medical, education.field_of_study, Adrenal Hyperplasia, Congenital, biology, business.industry, Biochemistry (medical), 21-Hydroxylase, Gender Identity, medicine.disease, Europe, Paediatric endocrinology, biology.protein, Female, Steroid 21-Hydroxylase, business, Developed country |
الوصف: | Despite over 50 yr of experience with steroid replacement therapy the management of congenital adrenal hyperplasia (CAH) remains difficult and clinical practice varies substantially throughout the world. To consider the evidence for best practice to formulate management guidelines and to consider innovative therapies The Lawson Wilkins Pediatric Endocrine Society (LWPES) and The European Society for Pediatric Endocrinology (ESPE) convened a meeting in Gloucester MA March 14-17 2002. The 40 participating physicians psychologists scientists and surgeons from 12 countries on 4 continents agreed with the following consensus statement; this statement is concerned exclusively with CAH caused by 21-hydroxylase deficiency and does not address the other rarer forms of CAH. (excerpt) |
تدمد: | 1945-7197 0021-972X |
الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::506c2eaf875749db6b3bd5f45b445f8bTest https://doi.org/10.1210/jc.2003-030127Test |
حقوق: | OPEN |
رقم الانضمام: | edsair.doi.dedup.....506c2eaf875749db6b3bd5f45b445f8b |
قاعدة البيانات: | OpenAIRE |
تدمد: | 19457197 0021972X |
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