AI Article Synopsis
- A mother and daughter are described as having specific medical characteristics including hypertelorism (wide-set eyes), mild limb defects, and an umbilical hernia/omphalocele.
- They also have natal teeth (teeth present at birth) and some minor craniofacial anomalies.
- This case indicates they are part of the third family documented with Teebi hypertelorism syndrome, which is a rare genetic condition inherited in an autosomal dominant pattern.
Article Abstract
We report a mother and daughter who have hypertelorism, mild limb defects, umbilical hernia/omphalocele, natal teeth and minor craniofacial anomalies. These individuals represent the third family with Teebi hypertelorism syndrome, a rare autosomal dominant syndrome.
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