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Braddock syndrome
rareBraddock syndrome is a rare malformation syndrome with multiple congenital abnormalities, described in 2 siblings, that is characterized by VACTERL -like association in combination with pulmonary hypertension, laryngeal webs, blue sclerae, abnormal ears, persistent growth deficiency and normal intellect.
- Identifiers
- MONDO:0012032 OMIM:608406Orphanet:52047
- Part of
- Multiple congenital anomalies/dysmorphic syndrome without intellectual disabilityPulmonary hypertension
- Also known as
- Vater-like syndrome with pulmonary hypertension, abnormal ears and growth deficiency
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