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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 1
1989 1
1990 1
1994 1
1999 2
2010 1
2011 1
2014 1
2017 1
2018 1
2019 2
2020 1
2021 1
2024 0

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14 results

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Page 1
Treatment of Common Congenital Hand Conditions.
Wang B, Tian X, Hu Y. Wang B, et al. Clin Plast Surg. 2019 Jul;46(3):489-503. doi: 10.1016/j.cps.2019.03.009. Epub 2019 Apr 20. Clin Plast Surg. 2019. PMID: 31103092 Review.
Using the new classification system proposed by Oberg, Manske and Tonkin (OMT) and endorsed by the International Federation of Societies for Surgery of the Hand, congenital hand differences are classified into malformations, deformations, and dysplasias and syndromes. Malformatio …
Using the new classification system proposed by Oberg, Manske and Tonkin (OMT) and endorsed by the International Federation of Societies for …
Postburn contractures of the hand.
Fufa DT, Chuang SS, Yang JY. Fufa DT, et al. J Hand Surg Am. 2014 Sep;39(9):1869-76. doi: 10.1016/j.jhsa.2014.03.018. J Hand Surg Am. 2014. PMID: 25154575 Review.
The most common and functionally limiting sequelae are contractures of the webspace, hand, and digits. Webspace contractures and postburn syndactyly are managed with scar excision and local soft tissue rearrangement or skin grafting. The burn claw hand presents as extensio …
The most common and functionally limiting sequelae are contractures of the webspace, hand, and digits. Webspace contractures and postburn …
A comprehensive review of reported heritable noggin-associated syndromes and proposed clinical utility of one broadly inclusive diagnostic term: NOG-related-symphalangism spectrum disorder (NOG-SSD).
Potti TA, Petty EM, Lesperance MM. Potti TA, et al. Hum Mutat. 2011 Aug;32(8):877-86. doi: 10.1002/humu.21515. Epub 2011 Jun 21. Hum Mutat. 2011. PMID: 21538686 Free article. Review.
The NOG gene encodes noggin, a secreted polypeptide that is important for regulating multiple signaling pathways during human development, particularly in cartilage and bone. The hallmark of NOG-related syndromes is proximal symphalangism, defined by abnormal fusion …
The NOG gene encodes noggin, a secreted polypeptide that is important for regulating multiple signaling pathways during human development, p …
Proximal symphalangism and congenital conductive hearing loss: otologic aspects.
Ensink RJ, Sleeckx JP, Cremers CW. Ensink RJ, et al. Am J Otol. 1999 May;20(3):344-9. Am J Otol. 1999. PMID: 10337976 Review.
OBJECTIVE: Results of stapedectomy are reported in a Belgian 26-year-old woman and two Dutch brothers having the proximal symphalangism syndrome (McKusick 18580). STUDY DESIGN: Case reports are presented. ...
OBJECTIVE: Results of stapedectomy are reported in a Belgian 26-year-old woman and two Dutch brothers having the proximal symphala …
Symphalangism in children. Case report and review of the literature.
Letts M, Davidson D, Beaulé P. Letts M, et al. Clin Orthop Relat Res. 1999 Sep;(366):178-85. Clin Orthop Relat Res. 1999. PMID: 10627733 Review.
The fusion can involve the proximal or the distal joints; however, involvement of the proximal interphalangeal joints is more common. ...The authors present the case of a 9-year-old boy with bilateral symphalangism of the proximal interphalangeal joint …
The fusion can involve the proximal or the distal joints; however, involvement of the proximal interphalangeal joints is more …
[The treatment of congenital foot abnormalities].
Blauth W. Blauth W. Z Orthop Ihre Grenzgeb. 1989 Jan-Feb;127(1):3-14. doi: 10.1055/s-2008-1040081. Z Orthop Ihre Grenzgeb. 1989. PMID: 2655332 Review. German.
As far as the rather frequent polydactylies are concerned, the author distinguishes between a distal phalanx type, an interphalanx type, a proximal phalanx type, a metatarsal type and a tarsal type, depending on the "level", each, where distal/proximal web separatio …
As far as the rather frequent polydactylies are concerned, the author distinguishes between a distal phalanx type, an interphalanx type, a …
Limb anomalies in chromosomal aberrations.
Pfeiffer RA, Santelmann R. Pfeiffer RA, et al. Birth Defects Orig Artic Ser. 1977;13(1):319-37. Birth Defects Orig Artic Ser. 1977. PMID: 322750 Review.
No entirely specific malformation type is seen. The most unusual malformation, aplasia of the thumbs with proximal synostosis of the 4th aand 5th metacarpals, is seen in 13q- (13r) but the precise cytogenetic basis is not clear. ...The question cannot yet be answered wheth …
No entirely specific malformation type is seen. The most unusual malformation, aplasia of the thumbs with proximal synostosis of the …
Is the Apert foot an overlooked aspect of this rare genetic disease? Clinical findings and treatment options for foot deformities in Apert syndrome.
Stauffer A, Farr S. Stauffer A, et al. BMC Musculoskelet Disord. 2020 Nov 28;21(1):788. doi: 10.1186/s12891-020-03812-2. BMC Musculoskelet Disord. 2020. PMID: 33248465 Free PMC article. Review.
BACKGROUND: Apert syndrome is characterised by the presence of craniosynostosis, midface retrusion and syndactyly of hands and feet, thus, synonymously referred to as acrocephalosyndactyly type I. ...Although the functional benefit of syndactyly separation in the fo …
BACKGROUND: Apert syndrome is characterised by the presence of craniosynostosis, midface retrusion and syndactyly of hands and feet, …
Symbrachydactyly: Finger nubbins are not always amniotic band disruption sequence.
Mills JK, Butler L, Mills EM, Oishi SN. Mills JK, et al. JAAPA. 2019 Apr;32(4):32-37. doi: 10.1097/01.JAA.0000553383.75260.0c. JAAPA. 2019. PMID: 30913147 Review.
ABDS usually affects more than one limb but symbrachydactyly largely is limited to one upper extremity, and has five distinct clinical presentations: short-fingered, atypical cleft, monodactylous, peromelic, and a forearm proximal transverse deficiency. This article discus …
ABDS usually affects more than one limb but symbrachydactyly largely is limited to one upper extremity, and has five distinct clinical prese …
A novel homozygous mutation in PVRL4 causes ectodermal dysplasia-syndactyly syndrome 1.
Florian R, Gruber R, Volc-Platzer B. Florian R, et al. Int J Dermatol. 2018 Feb;57(2):223-226. doi: 10.1111/ijd.13862. Epub 2017 Dec 19. Int J Dermatol. 2018. PMID: 29265343 Review.
One recently described rare entity is the autosomal recessive inherited ectodermal dysplasia-syndactyly syndrome 1 (EDSS1). Homozygous and compound heterozygous missense and nonsense mutations in the poliovirus receptor related-4 (PVRL4) gene, encoding cell adhesion molecu …
One recently described rare entity is the autosomal recessive inherited ectodermal dysplasia-syndactyly syndrome 1 (EDSS1). Homozygou …
14 results