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DOI 10.1007/s00431-013-2240-z

Медицинская библиотека · European journal of pediatrics · 2014

Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times.

Habel Alex, Herriot Richard, Kumararatne Dinakantha, Allgrove Jeremy, Baker Kate, Baxendale Helen, Bu'Lock Frances, Firth Helen, Gennery Andrew, Holland Anthony, Illingworth Claire, Mercer Nigel, Pannebakker Merel, Parry Andrew, Roberts Anne, Tsai-Goodman Beverly

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Аннотация

UNLABELLED: The commonest autosomal deletion, 22q11.2 deletion syndrome (22q11DS) is a multisystem disorder varying greatly in severity and age of identification between affected individuals. Holistic care is best served by a multidisciplinary team, with an anticipatory approach. Priorities tend to change with age, from feeding difficulties, infections and surgery of congenital abnormalities particularly of the heart and velopharynx in infancy and early childhood to longer-term communication, learning, behavioural and mental health difficulties best served by evaluation at intervals to consider and initiate management. Regular monitoring of growth, endocrine status, haematological and immune function to enable early intervention helps in maintaining health.

CONCLUSION

Guidelines to best practice management of 22q11DS based on a literature review and consensus have been developed by a national group of professionals with consideration of the limitations of available medical and educational resources.

Для цитирования: Habel Alex, Herriot Richard, Kumararatne Dinakantha, Allgrove Jeremy, Baker Kate, Baxendale Helen, Bu'Lock Frances, Firth Helen, Gennery Andrew, Holland Anthony, Illingworth Claire, Mercer Nigel, Pannebakker Merel, Parry Andrew, Roberts Anne, Tsai-Goodman Beverly. Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times.. European journal of pediatrics. 2014. DOI: 10.1007/s00431-013-2240-z.

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