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Quoted phrase not found in phrase index: "Clinodactyly of the thumb"
Page 1
Radial Polydactyly. What's New?
Perez-Lopez LM, la Iglesia DG, Cabrera-Gonzalez M. Perez-Lopez LM, et al. Curr Pediatr Rev. 2018;14(2):91-96. doi: 10.2174/1573396314666180124102012. Curr Pediatr Rev. 2018. PMID: 29366421 Review.
The Wassel classification is the universal classification for thumb duplication. One of the limitations of it is the misclassification of the immature epiphysis. ...Tada score is a validated functional scale that takes into account the most common and limiting compl …
The Wassel classification is the universal classification for thumb duplication. One of the limitations of it is the misclassificatio …
Oligodactyly with Thumb.
Baek GH, Kim J. Baek GH, et al. J Hand Surg Asian Pac Vol. 2016 Oct;21(3):283-91. doi: 10.1142/S2424835516400087. J Hand Surg Asian Pac Vol. 2016. PMID: 27595943
We also devised new classification system of oligodactyly based on the thumb deformities and locations of missing digits. RESULTS: Syndactyly among fingers was associated in four patients, clinodactyly caused by delta bone in one, hypoplasia of the thumb in o …
We also devised new classification system of oligodactyly based on the thumb deformities and locations of missing digits. RESULTS: Sy …
Clinical Characteristics and Surgical Outcomes of Congenital Ulnar-deviated Thumbs: Delta Triphalangeal Thumbs and Irregular Epiphyses.
Han B, Shen K, Wang Z, Xu Y. Han B, et al. J Pediatr Orthop. 2021 Jan;41(1):28-32. doi: 10.1097/BPO.0000000000001679. J Pediatr Orthop. 2021. PMID: 33086366 Free PMC article.
BACKGROUND: Delta triphalangeal thumbs (DTPT) and irregular epiphysis thumbs (IET) had different anatomic deformities. ...CONCLUSIONS: Ulnar clinodactyly of the thumb occurs because of different anatomic features such as DTPT or IET. ...
BACKGROUND: Delta triphalangeal thumbs (DTPT) and irregular epiphysis thumbs (IET) had different anatomic deformities. ...CONC …
The anatomy and management of the thumb in Apert syndrome.
Fereshetian S, Upton J. Fereshetian S, et al. Clin Plast Surg. 1991 Apr;18(2):365-80. Clin Plast Surg. 1991. PMID: 2065494
The thumb in a child with Apert syndrome provides the key to hand function. ...Along with the shortened and radially deviated proximal phalanx, the first webspace (thumb-index) is always deficient. This article details the authors' anatomic observations of th …
The thumb in a child with Apert syndrome provides the key to hand function. ...Along with the shortened and radially deviated proxima …
Leiomyoma of uterus in a patient with ring chromosome 12: case presentation and literature review.
Hajianpour MJ, Hajianpour AK, Habibian R, Wohlmuth C. Hajianpour MJ, et al. Am J Med Genet. 1996 May 17;63(2):335-9. doi: 10.1002/(SICI)1096-8628(19960517)63:2<335::AID-AJMG2>3.0.CO;2-S. Am J Med Genet. 1996. PMID: 8725781 Review.
We report on a 30-year-old women with de novo ring chromosome 12 mosaicism, 46,XX, r(12)(p13.3q24.3)/46,XX. In addition to the clinical manifestations generally observed in "ring syndrome" cases such as growth retardation, short stature, microcephaly, and mental deficiency …
We report on a 30-year-old women with de novo ring chromosome 12 mosaicism, 46,XX, r(12)(p13.3q24.3)/46,XX. In addition to the clinical mani …
Juberg-Hayward syndrome is a cohesinopathy, caused by mutation in ESCO2.
Kantaputra PN, Dejkhamron P, Intachai W, Ngamphiw C, Kawasaki K, Ohazama A, Krisanaprakornkit S, Olsen B, Tongsima S, Ketudat Cairns JR. Kantaputra PN, et al. Eur J Orthod. 2021 Jan 29;43(1):45-50. doi: 10.1093/ejo/cjaa023. Eur J Orthod. 2021. PMID: 32255174
RESULTS: Clinical findings of the patient consisted of repaired cleft lip/palate, microcephaly, ptosis, short stature, delayed bone age, hypoplastic fingers and thumbs, clinodactyly of the fifth fingers, and humeroradial synostosis leading to elbow restriction. ...P …
RESULTS: Clinical findings of the patient consisted of repaired cleft lip/palate, microcephaly, ptosis, short stature, delayed bone age, hyp …
Rubinstein-Taybi Syndrome in a 19-years old boy.
Zwierzchowski TJ, Przedborska A, Wilmańska I, Raczkowski JW. Zwierzchowski TJ, et al. Neuro Endocrinol Lett. 2015;36(5):417-20. Neuro Endocrinol Lett. 2015. PMID: 26707040
CASE: Craniofacial abnormalities including: microcephaly, underdeveloped maxilla, micrognathia, high arched palate, malocclusion, down-slanting palpebral fissures, thick eyelashes and full eyebrows. Clinodactyly, broad thumbs and toes were observed in the mus …
CASE: Craniofacial abnormalities including: microcephaly, underdeveloped maxilla, micrognathia, high arched palate, malocclusion, down-slant …
Exome sequencing in a patient with Catel-Manzke-like syndrome excludes the involvement of the known genes and reveals a possible candidate.
Stanghellini I, Dassi E, Bertorelli R, De Sanctis V, Caleffi A, Landi A, Percesepe A. Stanghellini I, et al. Eur J Med Genet. 2015 Nov;58(11):597-602. doi: 10.1016/j.ejmg.2015.09.010. Epub 2015 Sep 28. Eur J Med Genet. 2015. PMID: 26420031
In the present study we describe the exome sequencing and analysis of a patient with Catel-Manzke-like phenotype showing bilateral hyperphalangism of the second finger and thumb clinodactyly due to a unilateral delta phalanx, associated with growth, cardiac and vert …
In the present study we describe the exome sequencing and analysis of a patient with Catel-Manzke-like phenotype showing bilateral hyperphal …
Clinical quiz. Rubinstein-Taybi syndrome (synonyms: broad thumbs and great toes, characteristic facies, and mental retardation -- broad thumb-hallux syndrome).
Kanitakis J, Claudy A. Kanitakis J, et al. Eur J Dermatol. 2002 Jan-Feb;12(1):107, 108-9. Eur J Dermatol. 2002. PMID: 11809612
Physical examination revealed short stature, slight obesity, facial abnormalities (Fig. 1), short and broad thumbs and big toes (Figs. 2 and 3). A keloid was found on the right forearm, that had developed after surgical correction of a fracture (Fig. 4). ...Past medical hi …
Physical examination revealed short stature, slight obesity, facial abnormalities (Fig. 1), short and broad thumbs and big toes (Figs …
Syndrome of mild mental retardation, spastic gait, and skeletal malformations in a family with partial deficiency of hypoxanthine-guanine phosphoribosyltransferase.
Page T, Nyhan WL, Morena de Vega V. Page T, et al. Pediatrics. 1987 May;79(5):713-7. Pediatrics. 1987. PMID: 3575027
A syndrome has been observed in a kindred with deficient activity of hypoxanthine-guanine phosphoribosyltransferase in which affected hemizygotes have had mild mental retardation, a spastic gait, pyramidal tract signs, shortness of stature, proximally placed thumbs …
A syndrome has been observed in a kindred with deficient activity of hypoxanthine-guanine phosphoribosyltransferase in which affected …