| Literature DB >> 16506117 |
Akshaya Vachharajani1, Kathleen Bethin, Jean-Francois Mouillet, Yoel Sadovsky, Scott Saunders.
Abstract
A female infant (gestational age, 37 weeks) presented with respiratory distress and pulmonary hypertension. Incidental to her clinical course, she was discovered by abdominal ultrasound to have absent adrenal glands bilaterally. This is the first case report of congenitally absent adrenal glands noted at birth. The exons of the patient's SF-1 gene were sequenced, and despite identifying a single nucleotide polymorphism that preserves proline at position 125 of SF-1, none of the previously identified mutations were detected in our samples. The known role of SF-1 and its mutations in adrenal gland development are discussed.Entities:
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Year: 2006 PMID: 16506117 DOI: 10.1055/s-2006-931911
Source DB: PubMed Journal: Am J Perinatol ISSN: 0735-1631 Impact factor: 1.862