Total: 1 |
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PMID (PMCID) | ||
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24911853 |
MIXED_SAMPLE | |
The significance of molecular studies in the long-term follow-up of children with beckwith- wiedemann syndrome. | ||
Gizewska M, Wilk M, Patalan M, Mackay D, Peregud-Pegorzelski J, Gawrych E, Walczak M, Petriczko E, Brodkiewicz A. Turk J Pediatr. 2014;56(2):177-82. |
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Its clinical features are heterogeneous, including macrosomia, macroglossia, hemihyperplasia, abdominal wall defects, neonatal hypoglycemia, and increased risk of embryonal tumors such as Wilms tumor, adrenocortical carcinoma, hepatoblastoma, and neuroblastoma. |