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Zygodactyly type 1

MedGen UID:
377870
Concept ID:
C1853294
Disease or Syndrome
Synonym: Zygodactyly 1
 
Monarch Initiative: MONDO:0012351
OMIM®: 609815
Orphanet: ORPHA295187

Definition

Syndactyly type I (185900) is an autosomal dominant limb malformation characterized in its classical form by complete or partial webbing between the third and fourth fingers and/or the second and third toes. Zygodactyly is a subtype of type I syndactyly in which webbing of second and third toes occurs without hand involvement (summary by Malik et al., 2005). [from OMIM]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVZygodactyly type 1
Follow this link to review classifications for Zygodactyly type 1 in Orphanet.

Recent clinical studies

Etiology

Nor AM, Jagdeesh K, Mohd FAS, Kamraul AK, Yusmadi A, Noraslawati R, Malina O, Roziana R
Med J Malaysia 2023 Nov;78(6):756-762. PMID: 38031217
Faitatzidou D, Dipla K, Theodorakopoulou MP, Koutlas A, Tsitouridis A, Dimitriadis C, Pateinakis P, Zafeiridis A, Papagianni A, Jadoul M, Sarafidis P
Exp Biol Med (Maywood) 2023 Oct;248(20):1745-1753. Epub 2023 Nov 2 doi: 10.1177/15353702231198081. PMID: 37916412Free PMC Article
Muller L, Goh BS, Cordovés AP, Sargsyan G, Sikka K, Singh S, Qiu J, Xu L, Graham PL, James CJ, Greenham P
Int J Pediatr Otorhinolaryngol 2023 Jul;170:111583. Epub 2023 May 23 doi: 10.1016/j.ijporl.2023.111583. PMID: 37245391
Nopparat J, Khuituan P, Peerakietkhajorn S, Teanpaisan R
PLoS One 2023;18(4):e0284303. Epub 2023 Apr 11 doi: 10.1371/journal.pone.0284303. PMID: 37040355Free PMC Article
Malik S, Schott J, Ali SW, Oeffner F, Amin-ud-Din M, Ahmad W, Grzeschik KH, Koch MC
Eur J Hum Genet 2005 Dec;13(12):1268-74. doi: 10.1038/sj.ejhg.5201492. PMID: 16189548

Diagnosis

Kannikeswaran N, Spencer P, Carcone A, Huth M, Mehmood Y, Ellis D
J Asthma 2024 Apr;61(4):307-312. Epub 2023 Oct 25 doi: 10.1080/02770903.2023.2272796. PMID: 37847783Free PMC Article
Nor AM, Jagdeesh K, Mohd FAS, Kamraul AK, Yusmadi A, Noraslawati R, Malina O, Roziana R
Med J Malaysia 2023 Nov;78(6):756-762. PMID: 38031217
Delliaux S, Ichinose M, Watanabe K, Fujii N, Nishiyasu T
Pflugers Arch 2023 Apr;475(4):527-539. Epub 2023 Jan 16 doi: 10.1007/s00424-022-02780-x. PMID: 36645512
Czerninski R, Mordekovich N, Basile J
J Oral Pathol Med 2022 Sep;51(8):747-754. Epub 2022 Aug 23 doi: 10.1111/jop.13343. PMID: 36053963Free PMC Article
Gao R, Yan H, Duan J, Gao Y, Cao C, Li L, Guo L
Sci Rep 2022 Mar 22;12(1):4858. doi: 10.1038/s41598-022-08705-z. PMID: 35318355Free PMC Article

Therapy

Nor AM, Jagdeesh K, Mohd FAS, Kamraul AK, Yusmadi A, Noraslawati R, Malina O, Roziana R
Med J Malaysia 2023 Nov;78(6):756-762. PMID: 38031217
Adams JA, Lopez JR, Banderas V, Sackner MA
J Diabetes Res 2023;2023:4454396. Epub 2023 Apr 11 doi: 10.1155/2023/4454396. PMID: 37082380Free PMC Article
Nopparat J, Khuituan P, Peerakietkhajorn S, Teanpaisan R
PLoS One 2023;18(4):e0284303. Epub 2023 Apr 11 doi: 10.1371/journal.pone.0284303. PMID: 37040355Free PMC Article
Gao R, Yan H, Duan J, Gao Y, Cao C, Li L, Guo L
Sci Rep 2022 Mar 22;12(1):4858. doi: 10.1038/s41598-022-08705-z. PMID: 35318355Free PMC Article
Pfeiffer RA, Santelmann R
Birth Defects Orig Artic Ser 1977;13(1):319-37. PMID: 322750

Prognosis

Ching WY, Adhikari P, Jawad B, Podgornik R
Int J Mol Sci 2022 Sep 3;23(17) doi: 10.3390/ijms231710091. PMID: 36077490Free PMC Article
Czerninski R, Mordekovich N, Basile J
J Oral Pathol Med 2022 Sep;51(8):747-754. Epub 2022 Aug 23 doi: 10.1111/jop.13343. PMID: 36053963Free PMC Article
Malik S, Schott J, Ali SW, Oeffner F, Amin-ud-Din M, Ahmad W, Grzeschik KH, Koch MC
Eur J Hum Genet 2005 Dec;13(12):1268-74. doi: 10.1038/sj.ejhg.5201492. PMID: 16189548

Clinical prediction guides

Nor AM, Jagdeesh K, Mohd FAS, Kamraul AK, Yusmadi A, Noraslawati R, Malina O, Roziana R
Med J Malaysia 2023 Nov;78(6):756-762. PMID: 38031217
Loch Gomes R, Ribeiro F, Engrácia Valenti V, França Da Silva AK, Almeida Gonzaga L, Martins Pérego S, Luiz de Marco R, Marques Vanderlei LC
Altern Ther Health Med 2023 Mar;29(2):236-242. PMID: 33609347
Yıldırım Y, Ouriachi T, Woehlbier U, Ouahioune W, Balkan M, Malik S, Tolun A
Eur J Hum Genet 2018 Jun;26(6):876-885. Epub 2018 Mar 26 doi: 10.1038/s41431-018-0121-7. PMID: 29581481Free PMC Article
Malik S, Schott J, Ali SW, Oeffner F, Amin-ud-Din M, Ahmad W, Grzeschik KH, Koch MC
Eur J Hum Genet 2005 Dec;13(12):1268-74. doi: 10.1038/sj.ejhg.5201492. PMID: 16189548
Pfeiffer RA, Santelmann R
Birth Defects Orig Artic Ser 1977;13(1):319-37. PMID: 322750

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