Access to Multidisciplinary Care for Patients With 22q11.2 Deletion Syndrome: Identifying Breakdowns in the Screening Process
The 22q11.2 deletion syndrome affects approximately 1 in 4000 live births and involves cardiac defects, immunodeficiency, and endocrine disruption. The complexity of diagnosis and multifaceted care often leads to fragmented management in the short and long term. With the purpose of developing an eff...
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Published in: | The Journal of craniofacial surgery Vol. 31; no. 2; pp. 428 - 431 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
by Mutaz B. Habal, MD
01-03-2020
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Subjects: | |
Online Access: | Get full text |
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