Periventricular Nodular Heterotopia and Distal Limb Deficiency: A Recurrent Association

被引:3
作者
de Wit, Marie Claire Y. [2 ]
de Coo, Irenaeus F. M. [2 ]
Schot, Rachel [1 ]
Hoogeboom, A. Jeannette M. [1 ]
Lequin, Maarten H. [3 ]
Verkerk, Annemieke J. M. H. [4 ]
Mancini, Grazia M. S. [1 ]
机构
[1] Erasmus MC, Dept Clin Genet, NL-3000 CA Rotterdam, Netherlands
[2] Erasmus MC, Dept Neurol, NL-3000 CA Rotterdam, Netherlands
[3] Erasmus MC, Dept Radiol, NL-3000 CA Rotterdam, Netherlands
[4] Erasmus MC, Dept Bioinformat, NL-3000 CA Rotterdam, Netherlands
关键词
periventricular nodular heterotopia; malformations of cortical development; amniotic band; syndactyly; congenital hand malformation; congenital foot malformation; ADAMS-OLIVER-SYNDROME; APLASIA-CUTIS-CONGENITA; VASCULAR DISRUPTION; AMNIOTIC BANDS; ANOMALIES; BRAIN; SEQUENCE; VARIANT; DEFECTS; POLYMICROGYRIA;
D O I
10.1002/ajmg.a.33258
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Malformations of cerebral cortical development, in particular periventricular nodular heterotopia (PNH), and distal transverse limb deficiency have been reported as associated congenital anomalies. Patients with PNH and transverse limb deficiency can be classified as having amniotic band sequence or Adams-Oliver syndrome (AOS). Controversy exists whether these should be considered separate entities. In some AOS patients, autosomal recessive inheritance has been shown, but in most patients causes are unknown, and both environmental and genetic factors have been implicated. We present three patients with PNH and distal transverse limb deficiency to support the hypothesis that these should be considered part of one group of disorders, and highlight the variable severity of the clinical and neuroradiological phenotype. Chromosome abnormalities were excluded by copy number analysis on 250K SNP microarray data.Research done on limb deficiency as on PNH caused by mutations in known genes, suggests the involvement of vascular developmental pathways. The combination of limb deficiency and PNH may have a common causative mechanism. Recognition and grouping of patients with this combination of abnormalities will help elucidating the cause. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:954 / 959
页数:6
相关论文
共 39 条
[1]  
Amor DJ, 2000, AM J MED GENET, V93, P328, DOI 10.1002/1096-8628(20000814)93:4<328::AID-AJMG13>3.0.CO
[2]  
2-0
[3]   Total Synthesis and Biological Evaluation of Tubulysin U, Tubulysin V, and Their Analogues [J].
Balasubramanian, Ranganathan ;
Raghavan, Bhooma ;
Begaye, Adrian ;
Sackett, Dan L. ;
Fecik, Robert A. .
JOURNAL OF MEDICINAL CHEMISTRY, 2009, 52 (02) :238-240
[4]   SUBCLAVIAN ARTERY SUPPLY DISRUPTION SEQUENCE - HYPOTHESIS OF A VASCULAR ETIOLOGY FOR POLAND, KLIPPEL-FEIL, AND MOBIUS ANOMALIES [J].
BAVINCK, JNB ;
WEAVER, DD .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (04) :903-918
[5]   Aplasia cutis congenita, skull defect, brain heterotopia, and intestinal lymphangiectasia [J].
Bonioli, E ;
Hennekam, RC ;
Spena, G ;
Morcaldi, G ;
Di Stefano, A ;
Serra, G ;
Bellini, C .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 132A (02) :202-205
[6]   Abnormal neuronal migration defect in the severe variant subtype of Adams-Oliver syndrome [J].
Brancati, Francesco ;
Garaci, Francesco Giuseppe ;
Mingarelli, Rita ;
Dallapiccola, Bruno .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2008, 146A (12) :1622-1623
[7]   Periventricular neuronal heterotopia, oro-facio-digital anomalies, and microphthalmia. A new syndrome? [J].
Castro, CHBC ;
Freitas, PZ ;
Antoneli, MZ ;
Santiago, G ;
Ribeiro, LA ;
Richieri-Costa, A .
CLINICAL DYSMORPHOLOGY, 2005, 14 (04) :197-201
[8]   ACRANIA - A MANIFESTATION OF THE ADAMS-OLIVER SYNDROME [J].
CHITAYAT, D ;
MEUNIER, C ;
HODGKINSON, KA ;
ROBB, L ;
AZOUZ, M .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 44 (05) :562-566
[9]   Filamin A mutation, a common cause for periventricular heterotopia, aneurysms and cardiac defects [J].
de Wit, M. C. Y. ;
Kros, J. M. ;
Halley, D. J. J. ;
de Coo, I. F. M. ;
Verdijk, R. ;
Jacobs, B. C. ;
Mancini, G. M. S. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2009, 80 (04) :426-428
[10]   Cortical brain malformations - Effect of clinical, neuroradiological, and modern genetic classification [J].
de Wit, Marie Claire Yvette ;
Lequin, Maarten H. ;
de Coo, Ireneaus F. M. ;
Brusse, Esther ;
Halley, Dicky J. J. ;
van de Graaf, Raoul ;
Schot, Rachel ;
Verheijen, Frans W. ;
Mancini, Grazia M. S. .
ARCHIVES OF NEUROLOGY, 2008, 65 (03) :358-366