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Endocrine Abstracts

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49th Annual Meeting of the British Society for Paediatric Endocrinology and Diabetes

Belfast, Ireland
02 Nov 2022 - 04 Nov 2022

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49th Meeting of the British Society for Paediatric Endocrinology and Diabetes

Endocrine Main Meeting Sessions

Endocrine Symposium 1

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Endocrine Symposium 2

ea0085emm1.1 | Endocrine Symposium 1 | BSPED2022

Congenital imprinting disorders

Power Claire , Ann Lynch Sally , O hIci Bronagh , Connell Susan M O'

Congenital imprinting disorders (IDs) are a group of rare conditions affecting growth, metabolism and development caused by aberrant expression of imprinted genes in a parent-of-origin dependent manner. The internationally recognised IDs are Prader Willi Syndrome (PWS), Angelman Syndrome (AS), Beckwith Wiedemann Syndrome (BWS), Silver Russell Syndrome (SRS), Temple Syndrome (TS14), Pseudohypoparathyroidism (PHP), Transient Neonatal Diabetes Mellitus (TNDM) and Kagami-Ogata Syn...
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ea0085emm1.2 | Endocrine Symposium 1 | BSPED2022

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Published by BioScientifica

Endocrine Abstracts
ISSN 1470-3947 (print) | ISSN 1479-6848 (online)
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