The expanding panorama of split hand foot malformation

被引:24
作者
Basel, Donald [1 ]
Kilpatrick, Michael W. [1 ]
Tsipouras, Petros [1 ]
机构
[1] Univ Connecticut, Ctr Hlth, Dept Genet & Dev Biol, Farmington, CT 06030 USA
关键词
split hand foot malformation; SHFM;
D O I
10.1002/ajmg.a.31304
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The split hand/foot malformation is a developmental defect of the extremities resulting from errors in the initiation and maintenance of the apical ectodermal ridge. The phenotype is genetically heterogeneous, and it can be identified either as an isolated phenotypic manifestation or as a constituent component of a malformation syndrome. This overview describes the clinical phenotype, related animal models, and the evolving genetic heterogeneity of the malformation. (c) 2006 Wiley-Liss, Inc.
引用
收藏
页码:1359 / 1365
页数:7
相关论文
共 42 条
  • [1] X-CHROMOSOMALLY INHERITED SPLIT-HAND SPLIT-FOOT ANOMALY IN A PAKISTANI KINDRED
    AHMAD, M
    ABBAS, H
    HAQUE, S
    FLATZ, G
    [J]. HUMAN GENETICS, 1987, 75 (02) : 169 - 173
  • [2] Split hand foot malformation is associated with a reduced level of Dactylin gene expression
    Basel, D
    DePaepe, A
    Kilpatrick, MW
    Tsipouras, P
    [J]. CLINICAL GENETICS, 2003, 64 (04) : 350 - 354
  • [3] DELETION OF CHROMOSOME 2Q24-Q31 CAUSES CHARACTERISTIC DIGITAL ANOMALIES - CASE-REPORT AND REVIEW
    BOLES, RG
    POBER, BR
    GIBSON, LH
    WILLIS, CR
    MCGRATH, J
    ROBERTS, DJ
    YANGFENG, TL
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 55 (02): : 155 - 160
  • [4] Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome
    Celli, J
    Duijf, P
    Hamel, BCJ
    Bamshad, M
    Kramer, B
    Smits, APT
    Newbury-Ecob, R
    Hennekam, RCM
    Van Buggenhout, G
    van Haeringen, B
    Woods, CG
    van Essen, AJ
    de Waal, R
    Vriend, G
    Haber, DA
    Yang, A
    McKeon, F
    Brunner, HG
    van Bokhoven, H
    [J]. CELL, 1999, 99 (02) : 143 - 153
  • [5] DACTYLAPLASIA IN MICE - A 2-LOCUS MODEL FOR DEVELOPMENTAL ANOMALIES
    CHAI, CK
    [J]. JOURNAL OF HEREDITY, 1981, 72 (04) : 234 - 237
  • [6] Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse
    Crackower, M
    Motoyama, J
    Tsui, LC
    [J]. DEVELOPMENTAL BIOLOGY, 1998, 201 (01) : 78 - 89
  • [7] A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24
    de Mollerat, XJ
    Gurrieri, F
    Morgan, CT
    Sangiorgi, E
    Everman, DB
    Gaspari, P
    Amiel, J
    Bamshad, MJ
    Lyle, R
    Blouin, JL
    Allanson, JE
    Le Marec, B
    Wilson, M
    Braverman, NE
    Radhakrishna, U
    Delozier-Blanchet, C
    Abbott, A
    Elghouzzi, V
    Antonarakis, S
    Stevenson, RE
    Munnich, A
    Neri, G
    Schwartz, CE
    [J]. HUMAN MOLECULAR GENETICS, 2003, 12 (16) : 1959 - 1971
  • [8] P63 mutations are not a major cause of non-syndromic split hand/foot malformation
    de Mollerat, XJ
    Everman, DB
    Morgan, CT
    Clarkson, KB
    Rogers, RC
    Colby, RS
    Aylsworth, AS
    Graham, JM
    Stevenson, RE
    Schwartz, CE
    [J]. JOURNAL OF MEDICAL GENETICS, 2003, 40 (01) : 55 - 61
  • [9] Monodactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD cluster
    Del Campo, M
    Jones, MC
    Veraksa, AN
    Curry, CJ
    Jones, KL
    Mascarello, JT
    Ali-Kahn-Catts, Z
    Drumheller, T
    McGinnis, W
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (01) : 104 - 110
  • [10] Discrepancies in upper and lower limb patterning in split hand foot malformation
    Elliott, AM
    Reed, MH
    Roscioli, T
    Evans, JA
    [J]. CLINICAL GENETICS, 2005, 68 (05) : 408 - 423