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congenital absence of foot and toe (s)相关文献:
Fine Motor Disability.
Burr P, Choudhury P.
2022 Oct 10. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–.
PMID:33085413
Classification of Middle Phalangeal Postaxial Polysyndactyly Based on Intraoperative Arthrography Is Useful for Surgical Decision-making in Children Younger Than 2 Years.
Bae K, Kang MS, Kim TH, Park SS.
J Pediatr Orthop. 2021 Aug 1;41(7):437-443. doi: 10.1097/BPO.0000000000001858.
PMID:33999568
Novel Technique for Toe-to-Hand Transplantation: The Fourth-toe as an Alternative Option for Toe-to-Hand Transplantation for Pediatric Patients.
Ozols D, Zarins J, Petersons A.
Tech Hand Up Extrem Surg. 2019 Jun;23(2):74-80. doi: 10.1097/BTH.0000000000000234.
PMID:30720566
Toe-to-Hand Transfer in an Ulnar Hemimelia Patient: A Case Report.
Sönmez E, Aksam E.
Ann Plast Surg. 2019 Oct;83(4):436-438. doi: 10.1097/SAP.0000000000002011.
PMID:31524738
Anatomy of a duplicated human foot from a limb with fibular dimelia.
Rivera RE, Hootnick DR, Gingold AR, Levinsohn EM, Kruger LM, Packard DS Jr.
Teratology. 1999 Nov;60(5):272-82. doi: 10.1002/(SICI)1096-9926(199911)60:5<272::AID-TERA8>3.0.CO;2-E.
PMID:10525205
CASE-REPORT Low-level trisomy 14 mosaicism in a male newborn with ectrodactyly.
Rodrigues MA, Morgade LF, Dias LF, Moreira RV, Maia PD, Sales AF, Ribeiro PD.
Genet Mol Res. 2016 Dec 2;15(4). doi: 10.4238/gmr15049275.
PMID:27966762
Congenital Great Toe Hypoplasia Equivalent to a Grade 3 Hypoplastic Thumb in a Patient with VACTERL Association.
Mende K, Tonkin MA.
J Hand Surg Asian Pac Vol. 2018 Dec;23(4):605-606. doi: 10.1142/S2424835518720402.
PMID:30428812
Are triphalangeal thumb-polysyndactyly syndrome (TPTPS) and tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome (THPTTS) identical? A father with TPTPS and his daughter with THPTTS in a Thai family.
Kantaputra PN, Chalidapong P.
Am J Med Genet. 2000 Jul 17;93(2):126-31. doi: 10.1002/1096-8628(20000717)93:2<126::aid-ajmg9>3.0.co;2-s.
PMID:10869115
CHILD syndrome caused by a deletion of exons 6-8 of the NSDHL gene.
Kim CA, Konig A, Bertola DR, Albano LM, Gattás GJ, Bornholdt D, Leveleki L, Happle R, Grzeschik KH.
Dermatology. 2005;211(2):155-8. doi: 10.1159/000086448.
PMID:16088165
Brachydactyly type B: case report and further evidence for clinical heterogeneity.
Slavotinek A, Clayton-Smith J.
Clin Dysmorphol. 1999 Jul;8(3):165-71.
PMID:10457848
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