Publications by authors named "Stacy H Dowell"
BMJ Case Rep
November 2011
Article Synopsis
- - Goltz syndrome is a rare genetic disorder linked to the X chromosome that affects all three layers of embryonic development.
- - The symptoms can vary significantly, including anything from minor skin issues to the complete absence of limbs or organs.
- - Because it is so uncommon and presents in various ways, diagnosing Goltz syndrome can often be delayed or overlooked.
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