Disease #00203 (LDS4 (Loeys-Dietz syndrome, type 4 (LDS_4)), OMIM:614816)

Official abbreviation LDS4
Name Loeys-Dietz syndrome, type 4 (LDS_4)
OMIM ID 614816
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 3
Associated with 1 gene TGFB2
Associated tissues -
Disease features hypertelorism (HP:0000316); bifid uvula (HP:0000193)/cleft palate (HP:0000175); exotropia (HP:0000577); no craniosynostosis (-HP:0001363); no cervical spine instability (-HP:0010646); retrognathia (HP:0000278); scoliosis (HP:0002650); club foot (HP:0001762); osteoarthritis (HP:0002758); dural ectasia (HP:0100775); pneumothorax (HP:0002107); hernia (HP:0100790); dissection at young age; arterial tortuosity (HP:0005116)
Remarks -
Date created 2013-09-20 17:42:46 +02:00 (CEST)
Date last edited 2022-01-03 17:48:35 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00002976 FamPatII2 3-generation family, 5 affected (5M) - M no Germany white - - - - LDS4 aortic artery aneurysm, arterial tortuosity, scoliosis, foot deformity, retrognathia, hernia; aortic repair TGFB2 TGFB2 1 5 Georg Rosenberger
00081071 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - LDS4 Loeys-Dietz syndrome 4 (OMIM:614816) TGFB2 TGFB2 1 1 Daniel Trujillano
00245418 F24, I PubMed: Camerota 2019, Journal: Camerota 2019 - F no Italy - 48y - - - LDS4 - SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 - 1 1 Marco Ritelli
00286187 - - - - - - - - - - - LDS4 - TGFB2 TGFB2 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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