Compound heterozygous mutations in fibulin-4 causing neonatal lethal pulmonary artery occlusion, aortic aneurysm, arachnodactyly, and mild cutis laxa

Mutations involving elastic tissue proteins result in a broad spectrum of phenotypes affecting skin, skeleton, ocular and vascular structures, including tortuous blood vessels and cutis laxa. Here we report on a female newborn with apparently long fingers, aortic aneurysm, tortuous pulmonary arterie...

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Veröffentlicht in:American journal of medical genetics. Part A 2007-11, Vol.143A (22), p.2635-2641
Hauptverfasser: Dasouki, Majed, Markova, Dessislava, Garola, Robert, Sasaki, Takako, Charbonneau, Noe L., Sakai, Lynn Y., Chu, Mon-Li
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Sprache:eng
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