An autosomal dominant aneurysm with multisystem abnormalities caused by increased TGF-BETA signaling due to mutations in type I or II of TGF-BETA RECEPTOR. Additional craniofacial features include CLEFT PALATE; CRANIOSYNOSTOSIS; HYPERTELORISM; or bifid uvula. Phenotypes closely resemble MARFAN SYNDROME; Marfanoid craniosynostosis syndrome (Shprintzen-Goldberg syndrome); and EHLERS-DANLOS SYNDROME.
See also reference (FX) in Slovak
Ehlersov-Danlosov syndróm Marfanov syndróm
See also reference (FX) in English
Ehlers-Danlos Syndrome Marfan Syndrome
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(2) - MeSH descriptor
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