Disease #03437 (LDS3 (Loeys-Dietz syndrome, type 3 (LDS-3)), OMIM:613795)

Official abbreviation LDS3
Name Loeys-Dietz syndrome, type 3 (LDS-3)
OMIM ID 613795
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 6
Phenotype entries for this disease 4
Associated with 1 gene SMAD3
Associated tissues -
Disease features hypertelorism (HP:0000316); bifid uvula (HP:0000193)/cleft palate (HP:0000175); exotropia (HP:0000577); craniosynostosis (HP:0001363); 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 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-01-03 17:50:12 +01:00 (CET)


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00235311 - PubMed: Laterza 2019 - M no Italy - - - - - LDS3 - S100A1, SMAD2, SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 SMAD3 1 1 Marco Ritelli
00245414 F20, I PubMed: Camerota 2019, Journal: Camerota 2019 patient has an affected cousin carrying the same variant F no Italy - 31y - - - LDS3 - SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 SMAD3 1 2 Marco Ritelli
00245415 F21, I PubMed: Camerota 2019, Journal: Camerota 2019 patient has an affected mother, maternal uncle, and grandfather carrying variant M no Italy - 13y - - - LDS3 - SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 SMAD3 1 4 Marco Ritelli
00245416 F22, I PubMed: Camerota 2019, Journal: Camerota 2019 - F no Italy - 41y - - - LDS3 - SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 SMAD3 1 1 Marco Ritelli
00245417 F23, I PubMed: Camerota 2019, Journal: Camerota 2019 patient has an affected father carrying the same variant M no Italy - 23y - - - LDS3 - SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 SMAD3 1 2 Marco Ritelli
00296491 - - - - - - - - - - - LDS3 - SMAD3 SMAD3 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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