Literature DB >> 19125433

Elements of morphology: standard terminology for the hands and feet.

Leslie G Biesecker1, Jon M Aase, Carol Clericuzio, Fiorella Gurrieri, I Karen Temple, Helga Toriello.   

Abstract

An international group of clinicians working in the field of dysmorphology has initiated the standardization of terms used to describe human morphology. The goals are to standardize these terms and reach consensus regarding their definitions. In this way, we will increase the utility of descriptions of the human phenotype and facilitate reliable comparisons of findings among patients. Discussions with other workers in dysmorphology and related fields, such as developmental biology and molecular genetics, will become more precise. Here we introduce the anatomy of the hands and feet and define and illustrate the terms that describe the major characteristics of the hands and feet.

Entities:  

Mesh:

Year:  2009        PMID: 19125433      PMCID: PMC3224990          DOI: 10.1002/ajmg.a.32596

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  12 in total

1.  Lengths of the growing foot.

Authors:  M ANDERSON; M M BLAIS; W T GREEN
Journal:  J Bone Joint Surg Am       Date:  1956-10       Impact factor: 5.284

2.  A classification for congenital limb malformations.

Authors:  A B Swanson
Journal:  J Hand Surg Am       Date:  1976-07       Impact factor: 2.230

Review 3.  Clinical examination of the foot and ankle.

Authors:  Craig C Young; Mark W Niedfeldt; George A Morris; Kevin J Eerkes
Journal:  Prim Care       Date:  2005-03       Impact factor: 2.907

4.  A maneuver to assess the presence of metacarpal or metatarsal osseous syndactyly: a physical finding useful for the differential diagnosis of polydactyly.

Authors:  Leslie G Biesecker
Journal:  Am J Med Genet A       Date:  2007-08-01       Impact factor: 2.802

5.  Nail size in normal infants. Establishing standards for healthy term infants.

Authors:  B Seaborg; J Bodurtha
Journal:  Clin Pediatr (Phila)       Date:  1989-03       Impact factor: 1.168

6.  The human simian crease and its variants. A model for investigation of serious congenital malformation.

Authors:  E B Hook; R Bonenfant; M L Powers; M Greenberg; L R Shapiro
Journal:  Birth Defects Orig Artic Ser       Date:  1974

7.  Lower limb standards in newborns.

Authors:  P Merlob; Y Sivan; S H Reisner
Journal:  Am J Dis Child       Date:  1984-02

8.  Elements of morphology: standard terminology for the head and face.

Authors:  Judith E Allanson; Christopher Cunniff; H Eugene Hoyme; Julie McGaughran; Max Muenke; Giovanni Neri
Journal:  Am J Med Genet A       Date:  2009-01       Impact factor: 2.802

9.  Elements of morphology: standard terminology for the lips, mouth, and oral region.

Authors:  John C Carey; M Michael Cohen; Cynthia J R Curry; Koenraad Devriendt; Lewis B Holmes; Alain Verloes
Journal:  Am J Med Genet A       Date:  2009-01       Impact factor: 2.802

10.  Elements of morphology: standard terminology for the nose and philtrum.

Authors:  Raoul C M Hennekam; Valerie Cormier-Daire; Judith G Hall; Károly Méhes; Michael Patton; Roger E Stevenson
Journal:  Am J Med Genet A       Date:  2009-01       Impact factor: 2.802

View more
  24 in total

1.  Elements of morphology: standard terminology for the external genitalia.

Authors:  Raoul C M Hennekam; Judith E Allanson; Leslie G Biesecker; John C Carey; John M Opitz; Eric Vilain
Journal:  Am J Med Genet A       Date:  2013-05-06       Impact factor: 2.802

2.  Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes.

Authors:  Christina Halgren; Nete M Nielsen; Lusine Nazaryan-Petersen; Asli Silahtaroglu; Ryan L Collins; Chelsea Lowther; Susanne Kjaergaard; Morten Frisch; Maria Kirchhoff; Karen Brøndum-Nielsen; Allan Lind-Thomsen; Yuan Mang; Zahra El-Schich; Claire A Boring; Mana M Mehrjouy; Peter K A Jensen; Christina Fagerberg; Lotte N Krogh; Jan Hansen; Thue Bryndorf; Claus Hansen; Michael E Talkowski; Mads Bak; Niels Tommerup; Iben Bache
Journal:  Am J Hum Genet       Date:  2018-05-24       Impact factor: 11.025

3.  Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations.

Authors:  Jennifer J Johnston; Julie C Sapp; Joyce T Turner; David Amor; Salim Aftimos; Kyrieckos A Aleck; Maureen Bocian; Joann N Bodurtha; Gerald F Cox; Cynthia J Curry; Ruth Day; Dian Donnai; Michael Field; Ikuma Fujiwara; Michael Gabbett; Moran Gal; John M Graham; Peter Hedera; Raoul C M Hennekam; Joseph H Hersh; Robert J Hopkin; Hülya Kayserili; Alexa M J Kidd; Virginia Kimonis; Angela E Lin; Sally Ann Lynch; Melissa Maisenbacher; Sahar Mansour; Julie McGaughran; Lakshmi Mehta; Helen Murphy; Margarita Raygada; Nathaniel H Robin; Alan F Rope; Kenneth N Rosenbaum; G Bradley Schaefer; Amy Shealy; Wendy Smith; Maria Soller; Annmarie Sommer; Heather J Stalker; Bernhard Steiner; Mark J Stephan; David Tilstra; Susan Tomkins; Pamela Trapane; Anne Chun-Hui Tsai; Margot I Van Allen; Pradeep C Vasudevan; Bernhard Zabel; Janice Zunich; Graeme C M Black; Leslie G Biesecker
Journal:  Hum Mutat       Date:  2010-10       Impact factor: 4.878

4.  The development of a clinical screening instrument for tumour predisposition syndromes in childhood cancer patients.

Authors:  Saskia M J Hopman; Johannes H M Merks; Corianne A J M de Borgie; Cora M Aalfs; Leslie G Biesecker; Trevor Cole; Charis Eng; Eric Legius; Eamonn R Maher; Max M van Noesel; Alain Verloes; David H Viskochil; Anja Wagner; Rosanna Weksberg; Huib N Caron; Raoul C M Hennekam
Journal:  Eur J Cancer       Date:  2013-07-12       Impact factor: 9.162

5.  Assessment of congenital anomalies in infants born to pregnant women enrolled in clinical trials.

Authors:  Sonja A Rasmussen; Sonia Hernandez-Diaz; Omar A Abdul-Rahman; Leyla Sahin; Carey R Petrie; Kim M Keppler-Noreuil; Sharon E Frey; Robin M Mason; Mirjana Nesin; John C Carey
Journal:  Clin Infect Dis       Date:  2014-12-15       Impact factor: 9.079

6.  Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes.

Authors:  Shannon Marchegiani; Taylor Davis; Federico Tessadori; Gijs van Haaften; Francesco Brancati; Alexander Hoischen; Haigen Huang; Elise Valkanas; Barbara Pusey; Denny Schanze; Hanka Venselaar; Anneke T Vulto-van Silfhout; Lynne A Wolfe; Cynthia J Tifft; Patricia M Zerfas; Giovanna Zambruno; Ariana Kariminejad; Farahnaz Sabbagh-Kermani; Janice Lee; Maria G Tsokos; Chyi-Chia R Lee; Victor Ferraz; Eduarda Morgana da Silva; Cathy A Stevens; Nathalie Roche; Oliver Bartsch; Peter Farndon; Eva Bermejo-Sanchez; Brian P Brooks; Valerie Maduro; Bruno Dallapiccola; Feliciano J Ramos; Hon-Yin Brian Chung; Cédric Le Caignec; Fabiana Martins; Witold K Jacyk; Laura Mazzanti; Han G Brunner; Jeroen Bakkers; Shuo Lin; May Christine V Malicdan; Cornelius F Boerkoel; William A Gahl; Bert B A de Vries; Mieke M van Haelst; Martin Zenker; Thomas C Markello
Journal:  Am J Hum Genet       Date:  2015-06-25       Impact factor: 11.025

7.  Detailed assessment of the ear in Cornelia de Lange syndrome: comparison with a control sample using the new dysmorphology guidelines.

Authors:  Alasdair G W Hunter; Julianne S Collins; Matthew A Deardorff; Ian D Krantz
Journal:  Am J Med Genet A       Date:  2009-10       Impact factor: 2.802

8.  Elements of morphology: standard terminology for the head and face.

Authors:  Judith E Allanson; Christopher Cunniff; H Eugene Hoyme; Julie McGaughran; Max Muenke; Giovanni Neri
Journal:  Am J Med Genet A       Date:  2009-01       Impact factor: 2.802

9.  Elements of morphology: introduction.

Authors:  Judith E Allanson; Leslie G Biesecker; John C Carey; Raoul C M Hennekam
Journal:  Am J Med Genet A       Date:  2009-01       Impact factor: 2.802

10.  Dual Diagnosis of Ellis-van Creveld Syndrome and Hearing Loss in a Consanguineous Family.

Authors:  Barbara Vona; Reza Maroofian; Geetu Mendiratta; Matthew Croken; Siwu Peng; Xiaoqian Ye; Jamileh Rezazadeh; Paulina Bahena; Caroline Lekszas; Thomas Haaf; Lisa Edelmann; Lisong Shi
Journal:  Mol Syndromol       Date:  2017-09-22
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.