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2-5 finger syndactyly

MedGen UID:
869310
•Concept ID:
C4023736
•
Anatomical Abnormality

Recent clinical studies

Etiology

A variant of uncertain significance of the HMGA2 gene in a child with Silver-Russell syndrome-like phenotype: a case report.
Bourousis E, Xatzipsalti M, Polychroni I, Kanavakis E, Stamoyannou L
Hormones (Athens) 2024 Sep;23(3):591-593. Epub 2024 May 24 doi: 10.1007/s42000-024-00562-x. PMID: 38789914
Lower extremity postaxial polydactyly: Current literature status and future avenues.
Chocron Y, Kazan R, Abi-Rafeh J, Lessard A, Thibaudeau S
J Plast Reconstr Aesthet Surg 2021 Nov;74(11):2977-2992. Epub 2021 Apr 18 doi: 10.1016/j.bjps.2021.03.094. PMID: 33992559
Dorsal plane-shaped advancement flap for the reconstruction of web space in syndactyly without skin grafting: A preliminary report.
Liu J, Zheng H, Chen Z, Dai X, Schilling AF, Machens HG
J Plast Reconstr Aesthet Surg 2015 Nov;68(11):e167-73. Epub 2015 Jun 27 doi: 10.1016/j.bjps.2015.06.016. PMID: 26190763
Application of C-Shaped Osteotomy and Distraction Osteogenesis for Correction of Radial Angulation Deformities of the Hand in Children With Apert Syndrome: Review of 10 Years of Experience.
Vargel I, Calis M, Cavusoglu T, Ekin O, Oznur A
Ann Plast Surg 2015 Nov;75(5):513-7. doi: 10.1097/SAP.0000000000000353. PMID: 25275478
Congenital constriction band syndrome.
Askins G, Ger E
J Pediatr Orthop 1988 Jul-Aug;8(4):461-6. doi: 10.1097/01241398-198807000-00016. PMID: 2839541

Diagnosis

A variant of uncertain significance of the HMGA2 gene in a child with Silver-Russell syndrome-like phenotype: a case report.
Bourousis E, Xatzipsalti M, Polychroni I, Kanavakis E, Stamoyannou L
Hormones (Athens) 2024 Sep;23(3):591-593. Epub 2024 May 24 doi: 10.1007/s42000-024-00562-x. PMID: 38789914
Lower extremity postaxial polydactyly: Current literature status and future avenues.
Chocron Y, Kazan R, Abi-Rafeh J, Lessard A, Thibaudeau S
J Plast Reconstr Aesthet Surg 2021 Nov;74(11):2977-2992. Epub 2021 Apr 18 doi: 10.1016/j.bjps.2021.03.094. PMID: 33992559
Small reciprocal insertion detected by spectral karyotyping (SKY) and delimited by array-CGH analysis.
Matthaei A, Werner W, Gerlach EM, Koerner U, Tinschert S, Nitz I, Herr A, Rump A, Bartsch O, Hinkel KG, Schrock E, Oexle K
Eur J Med Genet 2005 Jul-Sep;48(3):328-38. doi: 10.1016/j.ejmg.2005.04.024. PMID: 16179228
Fanconi anemia complementation group E: clinical and cytogenetic data of the first patient.
Wegner RD, Henrichs I, Joenje H, Schroeder-Kurth T
Clin Genet 1996 Dec;50(6):479-82. doi: 10.1111/j.1399-0004.1996.tb02716.x. PMID: 9147877
Greig cephalopolysyndactyly syndrome. Report of a sporadic case.
Kunze J, Kaufmann HJ
Helv Paediatr Acta 1985;40(6):489-95. PMID: 3007398

Prognosis

Dorsal plane-shaped advancement flap for the reconstruction of web space in syndactyly without skin grafting: A preliminary report.
Liu J, Zheng H, Chen Z, Dai X, Schilling AF, Machens HG
J Plast Reconstr Aesthet Surg 2015 Nov;68(11):e167-73. Epub 2015 Jun 27 doi: 10.1016/j.bjps.2015.06.016. PMID: 26190763
Application of C-Shaped Osteotomy and Distraction Osteogenesis for Correction of Radial Angulation Deformities of the Hand in Children With Apert Syndrome: Review of 10 Years of Experience.
Vargel I, Calis M, Cavusoglu T, Ekin O, Oznur A
Ann Plast Surg 2015 Nov;75(5):513-7. doi: 10.1097/SAP.0000000000000353. PMID: 25275478
Distraction osteogenesis in the hand.
Pensler JM, Carroll NC, Cheng LF
Plast Reconstr Surg 1998 Jul;102(1):92-5. doi: 10.1097/00006534-199807000-00014. PMID: 9655412
Fanconi anemia complementation group E: clinical and cytogenetic data of the first patient.
Wegner RD, Henrichs I, Joenje H, Schroeder-Kurth T
Clin Genet 1996 Dec;50(6):479-82. doi: 10.1111/j.1399-0004.1996.tb02716.x. PMID: 9147877

Clinical prediction guides

A case report of Turner syndrome associated with fetal nuchal cystic hygroma and bilateral syndactyly of the hands and feet.
Chen HY, Zheng JQ, Zhang HP
Ital J Pediatr 2019 Jul 18;45(1):85. doi: 10.1186/s13052-019-0680-4. PMID: 31319890Free PMC Article
Application of C-Shaped Osteotomy and Distraction Osteogenesis for Correction of Radial Angulation Deformities of the Hand in Children With Apert Syndrome: Review of 10 Years of Experience.
Vargel I, Calis M, Cavusoglu T, Ekin O, Oznur A
Ann Plast Surg 2015 Nov;75(5):513-7. doi: 10.1097/SAP.0000000000000353. PMID: 25275478
Distraction osteogenesis in the hand.
Pensler JM, Carroll NC, Cheng LF
Plast Reconstr Surg 1998 Jul;102(1):92-5. doi: 10.1097/00006534-199807000-00014. PMID: 9655412

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