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Journal articles on the topic 'Clinodactyly'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 February 2022

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1

Le Mapihan, Marie, Alina Badina, Stéphanie Pannier, Arielle Salon, Chrisophe Glorion, and Stéphane Guero. "Non-vascularized toe phalanx transfer for correction of severe clinodactyly of the thumb in Rubinstein–Taybi syndrome." Journal of Hand Surgery (European Volume) 45, no. 7 (2020): 715–21. http://dx.doi.org/10.1177/1753193420909784.

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In Rubinstein–Taybi syndrome, patients may have a particularly severe clinodactyly of the thumb. We evaluated a new method for correction of these severe clinodactylies using non-vascularized toe phalanx transfer as a replacement for the abnormal delta phalanx. Results of the new technique are presented, together with those of an osteotomy technique. We retrospectively recorded the angle of the clinodactyly before and after surgery and at long-term follow-up of 11 osteotomies and five transfers in nine patients from 1990 to 2017. The pre-operative angle of clinodactyli was similar between the

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2

Moeller, Amy. "Clinodactyly." Techniques in Orthopaedics 34, no. 1 (2019): 18–25. http://dx.doi.org/10.1097/bto.0000000000000358.

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3

Goldfarb, Charles A., and Lindley B. Wall. "Osteotomy for Clinodactyly." Journal of Hand Surgery 40, no. 6 (2015): 1220–24. http://dx.doi.org/10.1016/j.jhsa.2015.03.003.

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4

WOOD, V. "Clinodactyly : An unusual presentation." Journal of Hand Surgery: Journal of the British Society for Surgery of the Hand 14, no. 4 (1989): 449–50. http://dx.doi.org/10.1016/0266-7681(89)90167-8.

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5

Roller, Jan. "Clinodactyly—Frequency and morphological implications." Plastic and Reconstructive Surgery 76, no. 6 (1985): 981. http://dx.doi.org/10.1097/00006534-198512000-00076.

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6

Sferopoulos, Nikolaos. "Congenital Clinodactyly of the Thumb." British Journal of Medicine and Medical Research 4, no. 15 (2014): 2874–83. http://dx.doi.org/10.9734/bjmmr/2014/8783.

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7

Gillis, Joshua A., Michael C. Nicoson, Lorena Floccari, Joseph S. Khouri, and Steven L. Moran. "Comparison of Vickers’ Physiolysis With Osteotomy for Primary Correction of Clinodactyly." HAND 15, no. 4 (2019): 472–79. http://dx.doi.org/10.1177/1558944719827999.

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Background: The purpose of this study was to compare the Vickers physiolysis procedure with osteotomy for correction of digital clinodactyly and determine which method provides better correction at final follow-up or whether the patient’s age, preoperative angulation, or presence of syndactyly affects final outcomes. Methods: All patients of skeletal immaturity who underwent surgical correction of clinodactyly were evaluated with clinical examination and radiographs to determine the percentage and absolute change in the degree of clinodactyly pre- versus postoperatively, in addition to stratif

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8

Almajidy, Arwa, and Sabah Naji. "http://www.iqnjm.com/wp-content/uploads/2020/01/Unmet-health-care-work-s-2-No..pdf." Iraqi National Journal of Medicine 2, no. 1 (2020): 42–51. http://dx.doi.org/10.37319/iqnjm.2.1.4.

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Background: Clinodactyly or inclination of the digits, particularly the fifth digit, is a congenital anomaly of the hand that occurs in 1% to 19.5% of the population. This deformity requires reconstruction of both the functional and the aesthetic appearance of the finger, if it is severe, to avoid future growth deformity. Objective: The study aims to review the outcomes and the complications associated with closing and reverse wedge osteotomy techniques for treating clinodactyly. Patients and Methods: Ten patients’ ten fingers with clinodactyly were submitted for reconstruction from March 2014

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9

Strauss, Nicole L., and Charles A. Goldfarb. "Surgical Correction of Clinodactyly: Two Straightforward Techniques." Techniques in Hand & Upper Extremity Surgery 14, no. 1 (2010): 54–57. http://dx.doi.org/10.1097/bth.0b013e3181d44078.

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10

Al-Qattan, M. M. "Congenital Sporadic Clinodactyly of the Index Finger." Annals of Plastic Surgery 59, no. 6 (2007): 682–87. http://dx.doi.org/10.1097/sap.0b013e318047c0c3.

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11

Caouette-Laberge, Louise, Caroline Laberge, E. Patricia Egerszegi, and Constantin Stanciu. "Physiolysis for correction of clinodactyly in children." Journal of Hand Surgery 27, no. 4 (2002): 659–65. http://dx.doi.org/10.1053/jhsu.2002.33702.

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12

Damen, A., B. van der Lei, and J. P. A. Nicolai. "Kirner's deformity and clinodactyly in one family." European Journal of Plastic Surgery 23, no. 4 (2000): 235–37. http://dx.doi.org/10.1007/s002380050259.

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13

Tengan, Célia H., Antonio C. Antunes, José R. Bauab, Gilmar F. Prado, Gilberto M. Manzano, and Alberto A. Gabbai. "Andersen syndrome: an association of periodic paralysis, cardiac arrhythmia and dysmorphic abnormalities." Arquivos de Neuro-Psiquiatria 64, no. 3a (2006): 582–84. http://dx.doi.org/10.1590/s0004-282x2006000400009.

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Andersen syndrome (AS) is a rare disease characterized by the presence of periodic paralysis (PP), cardiac arrhythmia and dysmorphic abnormalities. We report herein the first Brazilian patient presenting AS who also had obesity, obstructive sleep apnea (OSA) and daytime sleepiness. Clinical and genetic evaluation of six family members demonstrated that four had dysmorphic abnormalities but none had PP or cardiac arrhythmia. Sequencing of KCNJ2 revealed the R218W mutation in the index patient and her 6-year-old daughter, who presented dysmorphic abnormalities (micrognathia, clinodactyly of four

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14

Bednar, Michael S., Randip R. Bindra, and Terry R. Light. "Epiphyseal Bar Resection and Fat Interposition for Clinodactyly." Journal of Hand Surgery 35, no. 5 (2010): 834–37. http://dx.doi.org/10.1016/j.jhsa.2010.02.024.

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15

Lazzeri, Davide, Luca Grassetti, Giovanni di Benedetto, William R. Albury, and George M. Weisz. "The Hand in Art: Clinodactyly in Renaissance Paintings." Journal of Hand Surgery 40, no. 10 (2015): 2058–60. http://dx.doi.org/10.1016/j.jhsa.2015.05.004.

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16

Andrade, Carlos, Joana Meireles, Miguel Leão, and Fernando Silveira. "Clinodactyly and syndactyly – diagnostic clues for Andersen-Tawil syndrome." Arquivos de Neuro-Psiquiatria 72, no. 11 (2014): 899. http://dx.doi.org/10.1590/0004-282x20140168.

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17

Ali, Munawar, Teresa Jackson, and Ghazi M. Rayan. "Closing Wedge Osteotomy of Abnormal Middle Phalanx for Clinodactyly." Journal of Hand Surgery 34, no. 5 (2009): 914–18. http://dx.doi.org/10.1016/j.jhsa.2009.01.007.

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18

Medina, Jose A., Patrick Lorea, David Elliot, and Guy Foucher. "Correction of Clinodactyly by Early Physiolysis: 6-Year Results." Journal of Hand Surgery 41, no. 6 (2016): e123-e127. http://dx.doi.org/10.1016/j.jhsa.2016.02.006.

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19

Fairbank, S. M., W. M. Rozen, and C. J. Coombs. "The pathogenesis of Kirner’s deformity: A clinical, radiological and histological study." Journal of Hand Surgery (European Volume) 40, no. 6 (2014): 633–37. http://dx.doi.org/10.1177/1753193414551911.

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The distal phalanx in Kirner’s disease is abnormal and recognizable both clinically and radiologically. Despite previous investigation, the cause of these abnormalities is not clear. The current study seeks to evaluate the abnormal physis in Kirner’s deformity using radiological investigation, intraoperative observation and histopathological assessment in three clinical cases. Similarities with clinodactyly are described. Three patients with Kirner’s deformity underwent plain-film radiography and magnetic resonance imaging. Intraoperative observations were recorded, and histologic assessment o

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20

Zaheer, Arif, Faryad Hussain, Rizwan Gohar, MUZAMAL HUSSAIN, Muhammad Shahid, and AMIR RASHEED. "A CASE OF SILVER- RUSSEL SYNDROME PRESENTING WITH SHORT STATURE AND THE INFLUENCE OF GROWTH HORMONE ON GROWTH." Pakistan Postgraduate Medical Journal 31, no. 04 (2021): 210–14. http://dx.doi.org/10.51642/ppmj.v31i01.341.

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The Silver-Russell syndrome (SRS) is a rare heterogeneous genetic disorder whose pathogenesis remains controversial. The diagnosis is mainly based on the clinical association of characteristic signs, including intrauterine growth retardation, postnatal short stature, relative macrocephaly, triangular facies, clinodactyly of the fifth finger and asymmetry of the body. In this case report, we focused on a patient with SRS, who came to OPD clinic with failure to thrive and delayed speech. The child presented with evident poor height and weight gain, relative macrocephaly. The specific SRS feature

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21

Ravishanker, R., and AS Bath. "Distraction - A Minimally Invasive Technique for Treating Camptodactyly and Clinodactyly." Medical Journal Armed Forces India 60, no. 3 (2004): 227–30. http://dx.doi.org/10.1016/s0377-1237(04)80051-0.

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22

Song, Duhyun, Junhyuk Chung, Hye-Gyeong Shin, Soo-Jung Jung, and Jae-Ho Lee. "The Prevalence and Genetic Pattern of Clinodactyly in Korean Populations." Korean Journal of Physical Anthropology 29, no. 3 (2016): 99. http://dx.doi.org/10.11637/kjpa.2016.29.3.99.

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23

Malik, Sajid, Muhammad Afzal, Sumera Gul, Abdul Wahab, and Mahmud Ahmad. "Autosomal dominant syndrome of camptodactyly, clinodactyly, syndactyly, and bifid toes." American Journal of Medical Genetics Part A 152A, no. 9 (2010): 2313–17. http://dx.doi.org/10.1002/ajmg.a.33552.

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24

El Sayed, L., A. Salon, C. Glorion, and S. Guero. "Physiolysis for correction of clinodactyly with delta phalanx: Early improvement." Hand Surgery and Rehabilitation 38, no. 2 (2019): 125–28. http://dx.doi.org/10.1016/j.hansur.2018.12.002.

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25

Tajima, Tatsuya. "A BRIEF REVIEW AND A PROPOSAL FOR THE CLASSIFICATION OF THE CONGENITAL ANOMALIES OF THE UPPER LIMB: My Proposal for the Classification of Congenital Upper Limb Anomalies." Hand Surgery 01, no. 01 (1996): 63–68. http://dx.doi.org/10.1142/s0218810496000117.

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The evaluation of the international classification of congenital anomalies of the upper limb in the past 25 years is described. Syndactyly, cleft hand, and central polydactyly have the same embryological defect. Triphalangeal thumb and five fingered hand are unclassifiable, while camplodactyly, clinodactyly and haemangioma should not be grouped under “failure of differentiation of parts”. A new approach in classification is suggested.

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26

Spiteri, Bernice Sophie, Yanika Stafrace, and Jean Calleja-Agius. "Silver-Russell Syndrome: A Review." Neonatal Network 36, no. 4 (2017): 206–12. http://dx.doi.org/10.1891/0730-0832.36.4.206.

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AbstractSilver-Russell syndrome (SRS) is a rare congenital imprinting disorder. The genetic findings in SRS patients are heterogeneous and often sporadic. However, chromosomes 7, 11, and 17 are consistently involved in all individuals who meet the strict diagnostic criteria of SRS. There are many clinical features characteristic of SRS; the most common are low birth weight, short stature, triangular face, clinodactyly, relative macrocephaly, ear anomalies, and skeletal asymmetry.

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27

Zohar, Yuval, and Nelo Laurian. "Bifid condyle of the mandible with associated polythelia and manual anomalies." Journal of Laryngology & Otology 101, no. 12 (1987): 1315–19. http://dx.doi.org/10.1017/s0022215100103767.

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SummarySyndromes of oro-mandibular-skeletal anomalies are confusing by their ambiguous and overlapping components. It is our purpose to bring attention to a case comprising a group of anomalies: bifid mandibular condyle, asymmetric contralateral ascending ramus of the mandible, supernumerary nipples (polythelia), supernumerary-rudimentary postaxial sixth fingers and clinodactyly. The associated malformations presented do not correspond to any previous report. The case may therefore represent a new malformation syndrome.

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28

Albright, Steven B., Amy S. Xue, John C. Koshy, Robert C. Orth, and Larry H. Hollier. "Bilateral Proximal Delta Phalanges: An Unusual Presentation of Familial Congenital Clinodactyly." HAND 6, no. 3 (2011): 340–43. http://dx.doi.org/10.1007/s11552-011-9339-3.

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29

Piper, Samantha L., Charles A. Goldfarb, and Lindley Wall. "Outcomes of Opening Wedge Osteotomy to Correct Angular Deformity in Clinodactyly." Journal of Hand Surgery 39, no. 9 (2014): e18-e19. http://dx.doi.org/10.1016/j.jhsa.2014.06.052.

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30

Gillis, Joshua A. "Comparison of Vickers Physiolysis Versus Osteotomy for Primary Correction of Clinodactyly." Journal of Hand Surgery 43, no. 9 (2018): S58. http://dx.doi.org/10.1016/j.jhsa.2018.06.112.

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31

Dogan, Ali, A. Murat Kalender, Bekir Atik, Samet Karabulut, and Ahmet Sebik. "Giant clinodactyly and macrodactyly of the hand associated with carpal tunnel syndrome." Journal of Plastic Surgery and Hand Surgery 48, no. 6 (2014): 432–33. http://dx.doi.org/10.3109/2000656x.2013.812762.

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32

Evans, D. M., and N. K. James. "A bipedicled neurovascular step-advancement flap for soft tissue lengthening in clinodactyly." British Journal of Plastic Surgery 45, no. 5 (1992): 380–84. http://dx.doi.org/10.1016/0007-1226(92)90009-m.

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33

Barriga-Martín, A., L. M. Romero-Muñoz, D. Aquerreta-Beola, and S. Amillo-Garayoa. "Post-traumatic clinodactyly of the little finger in Basque hand-pelota players." Revista Española de Cirugía Ortopédica y Traumatología (English Edition) 64, no. 3 (2020): 160–66. http://dx.doi.org/10.1016/j.recote.2020.03.007.

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34

Pelias, M. Z., and M. C. Kinnebrew. "Autosomal dominant transmission of ankylosed teeth, abnormalities of the jaws, and clinodactyly." Clinical Genetics 27, no. 5 (2008): 496–500. http://dx.doi.org/10.1111/j.1399-0004.1985.tb00238.x.

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35

Zhang, Guochuan, Hiroyuki Kato, and Hiroshi Yamazaki. "PHYSIOLYSIS FOR CORRECTION OF THE DELTA PHALANX IN CLINODACTYLY OF THE BILATERAL LITTLE FINGERS." Hand Surgery 10, no. 02n03 (2005): 297–302. http://dx.doi.org/10.1142/s0218810405002917.

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We report the results of long-term follow-up after Vickers' physiolysis of the trapezoidal delta phalanx in a boy aged five year and six months with bilateral clinodactyly of the little finger. Radial deviation of the little finger was corrected from 36° to 15° on the left, and from 35° to 15° on the right at last follow-up six years and five months after surgery. The patient's parents were satisfied with the cosmetic appearance. X-ray film showed the abnormal distal epiphyses of the middle phalanges of the little fingers had disappeared.

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36

Colovati, Mileny E. S., Beatriz M. Grossi, Gabriela D. Nunes, et al. "Atypical Prader-Willi and 15q13.3 Microdeletion Syndromes in a Patient with an Unbalanced Translocation." Cytogenetic and Genome Research 158, no. 4 (2019): 192–98. http://dx.doi.org/10.1159/000501753.

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Prader-Willi syndrome (PWS) and recurrent 15q13.3 microdeletion syndrome can be caused by genomic rearrangements in the complex 15q11q13 chromosomal region. Here, we describe the first female child with PWS and 15q13.3 microdeletion syndrome resulting from an unusual 10.7-Mb deletion from 15pter to 15q13.3 due to an unbalanced de novo 15;19 translocation. The patient presents with hypotonia, microcephaly, developmental delay with lack of speech, intellectual disability, happy demeanor, clinodactyly of the 4th and 5th fingers, and dysmorphic facial features discordant for PWS and consistent wit

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37

Dindar, Tuğba, Soysal Bas, and Alpay Duran. "Congenital Familial Clinodactyly of Index Finger with Proximal Delta Phalanges and Ulnar Deviation." Journal of Hand and Microsurgery 09, no. 01 (2017): 039–40. http://dx.doi.org/10.1055/s-0036-1597910.

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38

Alshami, M. "Atypical plantar keratoderma, pachyonychia and clinodactyly in a patient with Rothmund-Thomson syndrome." Clinical and Experimental Dermatology 40, no. 2 (2014): 227–29. http://dx.doi.org/10.1111/ced.12476.

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39

de Chalain, Tristan, Roger Hudgins, Fernando Burstein, and Kim Armfield. "Combination of Unilateral Polydactyly, Syndactyly, and Clinodactyly with Occipitocervical Encephalocele and Vertebral Fusion." Annals of Plastic Surgery 33, no. 1 (1994): 86–89. http://dx.doi.org/10.1097/00000637-199407000-00018.

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40

Piper, Samantha L., Charles A. Goldfarb, and Lindley B. Wall. "Outcomes of Opening Wedge Osteotomy to Correct Angular Deformity in Little Finger Clinodactyly." Journal of Hand Surgery 40, no. 5 (2015): 908–13. http://dx.doi.org/10.1016/j.jhsa.2015.01.017.

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41

Sobel, E., S. Levitz, R. Cohen, R. Giorgini, and KT Jules. "Longitudinal epiphyseal bracket: associated foot deformities with implications for treatment." Journal of the American Podiatric Medical Association 86, no. 4 (1996): 147–55. http://dx.doi.org/10.7547/87507315-86-4-147.

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The longitudinal epiphyseal bracket is a rare ossification defect of bones of the hands and feet and results in an abnormal epiphysis that is C-shaped, longitudinally oriented, and vertically extends into the diaphysis. The longitudinal epiphyseal bracket may exist as an isolated deformity, but is commonly associated with digital deformities such as polydactyly, duplicated digits, congenital hallux varus, and clinodactyly. Five case histories of children with the longitudinal epiphyseal bracket in different bones of the foot are described with three distinct clinical presentations. The develop

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42

Aminabadi, Naser Asl, Azin Taghizadeh Ganji, Ali Vafaei, Maryam Pourkazemi, and Sina Ghertasi Oskouei. "Oculodentodigital Dysplasia: Disease Spectrum in an Eight-year-old Boy, His Parents and a Sibling." Journal of Clinical Pediatric Dentistry 33, no. 4 (2009): 337–41. http://dx.doi.org/10.17796/jcpd.33.4.0r02810u1533h168.

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Oculodentodigital dysplasia is an extremely rare autosomal dominant pleiotropic disorder, caused by mutations in the Connexin 43 gene (GJA1). Described here is a previously undiagnosed case of an 8-year-old boy with enamel and dentin hypoplasia and typical faces. In this presentation, many typical clinical and radiographical features of this condition are present. The characteristic features include a typical face, premature loss of primary teeth and odontodysplasia of permanent teeth, clinodactyly, ocular signs,and CNS involvement. To our knowledge, the case that we report here is the first c

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43

Tadini, Gianluca, Luisa Carlotta Rossi, Elisa Faure, et al. "A Second Case of Gobello Nevus Syndrome." Case Reports in Dermatology 8, no. 1 (2016): 85–90. http://dx.doi.org/10.1159/000445675.

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An uncommon type of epidermal nevus characterized by hyperpigmented hyperkeratotic bands following a Blaschko-linear pattern and generalized follicular hyperkeratosis were observed in a 17-year-old male patient who additionally showed tufted hair folliculitis on the scalp and clinodactyly of the fifth finger of both hands. The combination of epidermal nevus with skeletal abnormalities was first described by Gobello et al. [Dermatology 2000;201:51-55] as a new epidermal nevus syndrome that was named after the first author of this work. Our case shows identical clinical and histopathological fea

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44

Putra, Manesha, Melissa Hicks, and Jacques Abramowicz. "False Low-Risk Single Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in Pentasomy 49,XXXXY." American Journal of Perinatology Reports 08, no. 01 (2018): e4-e6. http://dx.doi.org/10.1055/s-0037-1621722.

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Abstract Introduction Pentasomy 49,XXXXY is a sex chromosome anomaly difficult to be diagnosed prenatally. We describe a patient of pentasomy 49,XXXXY with false low-risk results using a noninvasive prenatal screening (NIPS). A 30-year-old G1P0 woman presented at 336/7 weeks, secondary to sonographic fetal anomalies. She had low-risk NIPS at 136/7 weeks. Anatomy survey showed bilateral clubfeet, clinodactyly of the left fifth digit, micropenis, and echogenic bowel. Cytogenetics analysis revealed pentasomy 49,XXXXY syndrome. We report third-trimester sonographic features of a fetus with pentaso

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45

Sainz Arregui, J., J. Ortiz Lacorzana, R. San Sebastian Chueca, and A. Barrio. "Rubinstein-Taybi syndrome: description and treatment of a case with clinodactyly and “clubbed thumbs”." European Journal of Plastic Surgery 13, no. 4 (1990): 157–58. http://dx.doi.org/10.1007/bf00236368.

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46

Vickers, D. "Clinodactyly of the Little Finger: A Simple Operative Technique for Reversal of the Growth Abnormality." Journal of Hand Surgery 17, no. 6 (1992): 702. http://dx.doi.org/10.1016/0266-7681(92)90210-s.

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The traditional approach to clinodactyly has been either to accept the deformity or to perform an osteotomy. As an alternative to osteotomy, a resection of the mid-zone of the continuous epiphysis along with the underlying physis and its replacement by a fat graft (physiolysis) is simpler and allows further growth hi the phalanx. Twelve of these operations have been reviewed with a maximum follow-up of six years. Excellent functional and cosmetic results have been obtained. The renewed growth is manifest not only by an increase in length, but also by a decrease in the angular deformity and imp

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47

Elkoun, David, Vittorio Ferrari, François Deroussen, Marie-Christine Plancq, Céline Klein, and Richard Gouron. "Middle Phalangectomy for the Correction of Toe Clinodactyly With Longitudinal Epiphyseal Bracket in Young Children." Journal of Foot and Ankle Surgery 58, no. 5 (2019): 1002–5. http://dx.doi.org/10.1053/j.jfas.2018.12.030.

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48

Ty, Jennifer M., and Michelle A. James. "Failure of Differentiation: Part II (Arthrogryposis, Camptodactyly, Clinodactyly, Madelung Deformity, Trigger Finger, and Trigger Thumb)." Hand Clinics 25, no. 2 (2009): 195–213. http://dx.doi.org/10.1016/j.hcl.2008.12.003.

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49

VICKERS, D. "Clinodactyly of the little finger: A simple operative technique for reversal of the growth abnormality." Journal of Hand Surgery: Journal of the British Society for Surgery of the Hand 12, no. 3 (1987): 335–42. http://dx.doi.org/10.1016/0266-7681(87)90184-7.

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50

Reed, Umbertina Conti, Maria Bernardete Dutra Resende, Lúcio Gobbo Ferreira, et al. "King-Denborough Syndrome: report of two Brazilian cases." Arquivos de Neuro-Psiquiatria 60, no. 3B (2002): 739–41. http://dx.doi.org/10.1590/s0004-282x2002000500011.

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We report on two boys aged 2 and 6 years-old respectively with dysmorphic face, ptosis, down-slanting palpebral fissures, hypertelorism, epicanthic folds, low-set ears, malar hypoplasia, micrognathia, high-arched palate, clinodactyly, palmar simian line, pectus excavatum, winging of the scapulae, lumbar lordosis and mild thoracic scoliosis who present congenital hypotonia, slightly delayed motor development, diffuse joint hyperextensibility and mild proximal weakness. The muscle biopsy revealed minimal but identifiable changes represented by size fiber variability, type I fiber predominance an

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