Saal Bulas syndrome
From Wikipedia, the free encyclopedia
| Saal Bulas syndrome | |
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| Named after |
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Saal Bulas syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Saal Bulas syndrome, or a subtype of Saal Bulas syndrome, affects fewer than 200,000 people in the US population.
This syndrome consists of ectrodactyly or lobster-like hands, diaphragmatic hernia and absence of the corpus callosum.[1]
In addition to these the following problems may also be present.
- abnormal alimentary tract
- cardiac septal defect
- low hair line in front
- oligodactyly or missing fingers
- respiratory distress
- stillbirth/neonatal death
