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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 classic form by complete or partial webbing between the third and fourth fingers and/or the second and third toes. Malik et al. (2005) classified a subtype of type I syndactyly in which webbing of second and third toes occurs without hand involvement as 'zygodactyly.' [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

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
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
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
Dimitriev D, Indeykina O, Dimitriev A
Noise Health 2023 Jul-Sep;25(118):165-175. doi: 10.4103/nah.nah_15_22. PMID: 37815078Free PMC Article
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
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
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
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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