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Quoted phrase not found in phrase index: "Camptodactyly of finger"
Page 1
Obstetric US: watch the fetal hands.
Rypens F, Dubois J, Garel L, Fournet JC, Michaud JL, Grignon A. Rypens F, et al. Radiographics. 2006 May-Jun;26(3):811-29; discussion 830-1. doi: 10.1148/rg.263055113. Radiographics. 2006. PMID: 16702456 Review.
Malformations of the hand can be classified, according to the predominant anomaly, among the following categories: alignment abnormalities (clenched hand, camptodactyly, clinodactyly, hypokinesia, clubhand, phocomelia), thumb anomalies, abnormal size (macrodactyly, trident …
Malformations of the hand can be classified, according to the predominant anomaly, among the following categories: alignment abnormalities ( …
The distal arthrogryposes: delineation of new entities--review and nosologic discussion.
Hall JG, Reed SD, Greene G. Hall JG, et al. Am J Med Genet. 1982 Feb;11(2):185-239. doi: 10.1002/ajmg.1320110208. Am J Med Genet. 1982. PMID: 7039311 Review.
Fourteen propositi (seven familial cases, seven isolated cases) had a newly recognized form of arthrogryposis, which we have designated distal arthrogryposis type 1, with the predominant manifestations of autosomal dominant inheritance; tightly clenched fists at birth, with media …
Fourteen propositi (seven familial cases, seven isolated cases) had a newly recognized form of arthrogryposis, which we have designated dist …
Congenital contractural arachnodactyly (Beals syndrome).
Viljoen D. Viljoen D. J Med Genet. 1994 Aug;31(8):640-3. doi: 10.1136/jmg.31.8.640. J Med Genet. 1994. PMID: 7815423 Free PMC article. Review.
The clinical features are marfanoid habitus, arachnodactyly, crumpled ears, camptodactyly of the fingers and adducted thumbs, mild contractures of the elbows, knees, and hips, and mild muscle hypoplasia especially of the calf muscles. ...Linkage to a gene coding for …
The clinical features are marfanoid habitus, arachnodactyly, crumpled ears, camptodactyly of the fingers and adducted thumbs, …
Evaluation of a stepwise surgical approach to camptodactyly.
Hamilton KL, Netscher DT. Hamilton KL, et al. Plast Reconstr Surg. 2015 Mar;135(3):568e-576e. doi: 10.1097/PRS.0000000000000958. Plast Reconstr Surg. 2015. PMID: 25719721
BACKGROUND: Camptodactyly is common, but its treatment remains controversial. Multiple deforming forces have been implicated in its pathogenesis. This study evaluates a logical clinical assessment and corresponding stepwise surgical plan. METHODS: Eighteen consecutive f …
BACKGROUND: Camptodactyly is common, but its treatment remains controversial. Multiple deforming forces have been implicated in its p …
Autosomal dominant syndrome of camptodactyly, clinodactyly, syndactyly, and bifid toes.
Malik S, Afzal M, Gul S, Wahab A, Ahmad M. Malik S, et al. Am J Med Genet A. 2010 Sep;152A(9):2313-7. doi: 10.1002/ajmg.a.33552. Am J Med Genet A. 2010. PMID: 20683984
We report on a 25-year follow-up of a Pakistani kindred with a unique combination of camptodactyly and clinodactyly of 5th fingers, mesoaxial camptodactyly of toes, and ulnar deviation of 3rd fingers. ...
We report on a 25-year follow-up of a Pakistani kindred with a unique combination of camptodactyly and clinodactyly of 5th fingers …
Rare Case of Pyoderma Gangrenosum in the Setting of PAPA Syndrome in a 12-Year-Old Child.
Alhumam A. Alhumam A. Int J Low Extrem Wounds. 2023 Sep;22(3):620-624. doi: 10.1177/15347346211036023. Epub 2021 Aug 12. Int J Low Extrem Wounds. 2023. PMID: 34382449
Local therapy with a foam dressing, topical steroid in the wound margin, and class II compression stockings showed no effect. The pediatric rheumatologist evaluated the ulcer with a camptodactyly of digit 5, subluxation of the wrists on both sides, and symmetric ulnar devi …
Local therapy with a foam dressing, topical steroid in the wound margin, and class II compression stockings showed no effect. The pediatric …
An infant with congenital respiratory insufficiency and diaphragmatic paralysis: A novel BICD2 phenotype?
Chin HL, Huynh S, Ashkani J, Castaldo M, Dixon K, Selby K, Shen Y, Wright M, Boerkoel CF, Hendson G, Jones SJM. Chin HL, et al. Am J Med Genet A. 2022 Mar;188(3):926-930. doi: 10.1002/ajmg.a.62578. Epub 2021 Nov 26. Am J Med Genet A. 2022. PMID: 34825470
We report an infant with congenital respiratory insufficiency requiring mechanical ventilation, congenital diaphragmatic paralysis, decreased lung volume, and single finger camptodactyly. The infant displayed appropriate antigravity limb movements but had radiological, ele …
We report an infant with congenital respiratory insufficiency requiring mechanical ventilation, congenital diaphragmatic paralysis, decrease …
Effect of passive stretching on simple camptodactyly in children younger than three years of age.
Rhee SH, Oh WS, Lee HJ, Roh YH, Lee JO, Baek GH. Rhee SH, et al. J Hand Surg Am. 2010 Nov;35(11):1768-73. doi: 10.1016/j.jhsa.2010.07.032. J Hand Surg Am. 2010. PMID: 21050962
PURPOSE: To present the effectiveness of passive stretching as a treatment for camptodactyly, without any other form of physiotherapy or splinting. ...CONCLUSIONS: Passive stretching can effectively improve flexion deformity in camptodactyly in infants and young chi …
PURPOSE: To present the effectiveness of passive stretching as a treatment for camptodactyly, without any other form of physiotherapy …
Congenital contractural arachnodactyly suspected by abnormally long extremities by fetal ultrasound.
Miyake R, Ichikawa M, Naruse K. Miyake R, et al. BMJ Case Rep. 2021 Mar 1;14(3):e237904. doi: 10.1136/bcr-2020-237904. BMJ Case Rep. 2021. PMID: 33649036 Free PMC article.
CCA is easily differentiated from MFS after birth due to the flexion of multiple joints, including elbows, knees, hips and fingers. During the fetal period, observation of arachnodactyly and folded fingers by fetal ultrasound is the means of differential diagnosis b …
CCA is easily differentiated from MFS after birth due to the flexion of multiple joints, including elbows, knees, hips and fingers. D …
ACVR1 (587T>C) mutation in a variant form of fibrodysplasia ossificans progressiva: second report.
Nakahara Y, Katagiri T, Ogata N, Haga N. Nakahara Y, et al. Am J Med Genet A. 2014 Jan;164A(1):220-4. doi: 10.1002/ajmg.a.36219. Epub 2013 Nov 20. Am J Med Genet A. 2014. PMID: 24259422 Review.
The clinical symptoms were similar to those reported previously: the delayed onset with a slower and mild clinical course and little finger camptodactyly. Gene analysis revealed that the patient was heterozygous for ACVR1 (587T>C) mutation, the same one as report …
The clinical symptoms were similar to those reported previously: the delayed onset with a slower and mild clinical course and little …
30 results