Mandibulofacial Syndrome With Growth and Mental Retardation, Microcephaly, Ear Anomalies With Skin Tags, and Cleft Palate in a Mother and Her Son: Autosomal Dominant or X-Linked Syndrome?

被引:16
|
作者
Guion-Almeida, Maria Leine [1 ]
Vendramini-Pittoli, Siulan [1 ]
Santos Passos-Bueno, Maria Rita [2 ]
Zechi-Ceidei, Roseli Maria [1 ]
机构
[1] Univ Sao Paulo, HRAC, Dept Clin Genet, BR-17012900 Bauru, SP, Brazil
[2] Univ Sao Paulo, Inst Biosci, Ctr Human Genome, Dept Genet & Evolutionary Biol, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
mandibulofacial dysostosis; branchial arch; speech delay; TREACHER-COLLINS-SYNDROME; DYSOSTOSIS; MUTATION; TCOF1;
D O I
10.1002/ajmg.a.32816
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on a Brazilian mother and her son affected with mandibulofacial dysostosis, growth and mental retardation, microcephaly, first branchial arch anomalies, and cleft palate. To date only three males and one female, all sporadic cases, with a similar condition have been reported. This article describes the first familial case with this rare condition indicating autosomal dominant or X-linked inheritance. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:2762 / 2764
页数:3
相关论文
共 36 条
  • [1] A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate
    Guion-Almeida, Maria Leine
    Zechi-Ceide, Roseli Maria
    Vendramini, Siulan
    Tabith, Alfredo Junior
    CLINICAL DYSMORPHOLOGY, 2006, 15 (03) : 171 - 174
  • [2] Multiple congenital anomalies syndrome: Growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients
    Guion-Almeida, ML
    Zechi-Ceide, RM
    Richieri-Costa, A
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1999, 87 (01): : 72 - 77
  • [3] Autosomal Dominant Syndrome of Mental Retardation, Hypotelorism, and Cleft Palate Resembling Schilbach-Rott Syndrome
    Shkalim, Vared
    Baris, Hagit N.
    Gal, Gavriel
    Gleiss, Ruth
    Calderon, Shlomo
    Wessels, Marja
    Maat-Kievit, Anneke
    Menten, Bjoern
    De Baere, Elfride
    Hennekam, Raoul C. M.
    Schirmacher, Anja
    Bale, Sherri
    Shohat, Mordechai
    Willems, Patrick J.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2009, 149A (12) : 2700 - 2705
  • [4] AN AUTOSOMAL DOMINANT SYNDROME OF UVEAL COLOBOMATA, CLEFT-LIP AND PALATE, AND MENTAL-RETARDATION
    KINGSTON, HM
    HARPER, PS
    JONES, PW
    JOURNAL OF MEDICAL GENETICS, 1982, 19 (06) : 444 - 446
  • [5] AN X-LINKED SYNDROME WITH MICROCEPHALY, SEVERE MENTAL-RETARDATION, SPASTICITY, EPILEPSY AND DEAFNESS
    RENIER, WO
    GABREELS, FJM
    JASPER, HHJ
    HUSTINX, TWJ
    GEELEN, JAG
    VANHAELST, UJG
    JOURNAL OF MENTAL DEFICIENCY RESEARCH, 1982, 26 (MAR): : 27 - 40
  • [6] Characterization of a New X-Linked Mental Retardation Syndrome With Microcephaly, Cortical Malformation, and Thin Habitus
    du Souich, Christele
    Chou, Athena
    Yin, Jingyi
    Oh, Tracey
    Nelson, Tanya N.
    Hurlburt, Jane
    Arbour, Laura
    Friedlander, Robin
    McGillivray, Barbara C.
    Tyshchenko, Nataliya
    Rump, Andreas
    Poskitt, Kenneth J.
    Demos, Michelle K.
    Van Allen, Margot I.
    Boerkoel, Cornelius F.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2009, 149A (11) : 2469 - 2478
  • [7] A NEW X-LINKED MULTIPLE CONGENITAL-ANOMALIES MENTAL-RETARDATION SYNDROME
    GOLABI, M
    ITO, M
    HALL, BD
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 17 (01): : 367 - 374
  • [8] X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28
    Armfield, K
    Nelson, R
    Lubs, HA
    Häne, B
    Schroer, RJ
    Arena, F
    Schwartz, CE
    Stevenson, RE
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1999, 85 (03): : 236 - 242
  • [9] DISTINCTIVE AUTOSOMAL OR X-LINKED DOMINANT SYNDROME OF MICROCEPHALY, MILD DEVELOPMENTAL DELAY, SHORT STATURE, AND DISTINCTIVE FACE
    WINTER, RM
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 47 (06): : 917 - 920
  • [10] MENTAL-RETARDATION, CONGENITAL HEART DEFECT, CLEFT-PALATE, SHORT STATURE, AND FACIAL ANOMALIES - A NEW X-LINKED MULTIPLE CONGENITAL-ANOMALIES MENTAL-RETARDATION SYNDROME - CLINICAL DESCRIPTION AND MOLECULAR STUDIES
    HAMEL, BCJ
    MARIMAN, ECM
    VANBEERSUM, SEC
    SCHOONBROODLENSSEN, AMJ
    ROPERS, HH
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 51 (04): : 591 - 597