Abstract：
:Children with congenital anomalies often represent a special diagnostic and management challenge. To provide optimal care for these children, one must employ a systematic approach to identify the likely pathogenic mechanism leading to the birth defects present. Determining how distinct anomalies relate to one another may lead to elucidation of a specific genetic etiology for the patient's condition. Genetic testing is increasingly available to allow for diagnostic confirmation. Using this systematic approach to a child with congenital anomalies permits accurate prognostic and recurrence risk counseling, informed management decisions, and the appropriate allocation of social support and medical resources.
journal_name
Prim Carejournal_title
Primary careauthors
Falk MJ,Robin NHdoi
10.1016/j.pop.2004.04.015keywords:
subject
Has Abstractpub_date
2004-09-01 00:00:00pages
605-19, xissue
3eissn
0095-4543issn
1558-299Xpii
S0095454304000582journal_volume
31pub_type
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