A review of supernumerary and absent limbs and digits of the upper limb

被引:1
作者
Klaassen, Zachary [1 ]
Choi, Monica [1 ]
Musselman, Ruth [1 ]
Eapen, Deborah [1 ]
Tubbs, R. Shane [2 ]
Loukas, Marios [1 ,3 ]
机构
[1] St Georges Univ, Dept Anat Sci, Sch Med, St Georges, Grenada
[2] Childrens Hosp, Sect Pediat Neurosurg, Birmingham, AL USA
[3] Univ Varmia & Masuria, Dept Anat, Fac Med, Olsztyn, Poland
关键词
Anatomy; Embryology; Amelia; Phocomelia; Supernumerary limbs; Accessory limbs; ROBERTS-SYNDROME; TETRA-AMELIA; MULTIPLE MALFORMATIONS; PULMONARY HYPOPLASIA; SC PHOCOMELIA; TETRAAMELIA; ANOMALIES; GENITALIA; HANDS; FEET;
D O I
10.1007/s00276-011-0871-1
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
For years people have been enamored by anomalies of the human limbs, particularly supernumerary and absent limbs and digits. Historically, there are a number of examples of such anomalies, including royal families of ancient Chaldea, tribes from Arabia, and examples from across nineteenth century Europe. The development of the upper limbs in a growing embryo is still being elucidated with the recent advent of homeobox genes, but researchers agree that upper limbs develop between stages 12-23 through a complex embryological process. Maternal thalidomide intake during limb development is known to cause limb reduction and subsequent amelia or phocomelia. Additionally, a number of clinical reports have illustrated different limb anomaly cases, with each situation unique in phenotype and developmental abnormality. Supernumerary and absent limbs and digits are not unique to humans, and a number of animal cases have also been reported. This review of the literature illustrates the historical, anatomical, and clinical aspects of supernumerary and absent limbs and digits for the upper limb.
引用
收藏
页码:101 / 106
页数:6
相关论文
共 43 条
[21]  
MartinezFrias ML, 1997, AM J MED GENET, V73, P189, DOI 10.1002/(SICI)1096-8628(19971212)73:2<189::AID-AJMG15>3.0.CO
[22]  
2-M
[23]  
Ming JE, 1997, AM J MED GENET, V72, P210, DOI 10.1002/(SICI)1096-8628(19971017)72:2<210::AID-AJMG16>3.0.CO
[24]  
2-Q
[25]   Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family [J].
Niemann, S ;
Zhao, CF ;
Pascu, F ;
Stahl, U ;
Aulepp, U ;
Niswander, L ;
Weber, JL ;
Müller, U .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (03) :558-563
[26]  
Ohro Y, 1998, CLIN GENET, V54, P52
[27]  
Pfeiffer R A, 1977, Birth Defects Orig Artic Ser, V13, P319
[28]   Ectromelia in Morelet's crocodile from Belize [J].
Rainwater, TR ;
McMurry, ST ;
Platt, SG .
JOURNAL OF WILDLIFE DISEASES, 1999, 35 (01) :125-129
[29]  
Roberts J., 1919, Ann Surg, V70, P252
[30]  
ROMKE C, 1987, CLIN GENET, V31, P170