Growth patterns of patients with 1p36 deletion syndrome

被引:5
作者
Sangu, Noriko [1 ,2 ]
Shimojima, Keiko [2 ]
Shimada, Shino [2 ,3 ]
Ando, Tomohiro [1 ]
Yamamoto, Toshiyuki [2 ]
机构
[1] Tokyo Womens Med Univ, Sch Med, Dept Oral & Maxillofacial Surg, Tokyo 1628666, Japan
[2] Tokyo Womens Med Univ, Inst Integrated Med Sci, Tokyo 1628666, Japan
[3] Tokyo Womens Med Univ, Dept Pediat, Tokyo 1628666, Japan
关键词
1p36 deletion syndrome; growth pattern; hyperphagia; obesity; subtelomeric deletion; WILLI-LIKE PHENOTYPE; MONOSOMY; 1P36; HYPERPHAGIA; OBESITY;
D O I
10.1111/cga.12029
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
1p36 deletion syndrome is one of the most common subtelomeric deletion syndromes. Obesity is frequently observed in patients with this syndrome. Thus, it is important to evaluate the growth status of an individual patient. For this purpose, we accumulated recorded growth data from 44 patients with this syndrome and investigated the growth patterns of patients. Most of the patients showed weight parameters within normal limits, whereas a few of these patients showed intrauterine growth delay and microcephaly. The length of the patients after birth was under the 50th centile in most patients. Many patients showed poor weight gain after birth, and only two female patients were overweight. These findings indicate two different phenotypes of the 1p36 deletion syndrome. The overweight patients with 1p36 deletion started excessive weight gain after two years of life. This characteristic of the patients with 1p36 deletion syndrome is similar to Prader-Willi syndrome.
引用
收藏
页码:82 / 86
页数:5
相关论文
共 14 条
[1]   Further delineation of deletion 1p36 syndrome in 60 patients: A recognizable phenotype and common cause of developmental delay and mental retardation [J].
Battaglia, Agatino ;
Hoyme, H. Eugene ;
Dallapiccola, Bruno ;
Zackai, Elaine ;
Hudgins, Louanne ;
McDonald-McGinn, Donna ;
Bahi-Buisson, Nadia ;
Romano, Corrado ;
Williams, Charles A. ;
Braley, Lisa L. ;
Zuberi, Sameer M. ;
Carey, John C. .
PEDIATRICS, 2008, 121 (02) :404-410
[2]   Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems [J].
D'Angelo, Carla S. ;
Da Paz, Jose A. ;
Kim, Chong A. ;
Bertola, Debora R. ;
Castro, Claudia I. E. ;
Varela, Monica C. ;
Koiffmann, Celia P. .
EUROPEAN JOURNAL OF MEDICAL GENETICS, 2006, 49 (06) :451-460
[3]   Extending the Phenotype of Monosomy 1p36 Syndrome and Mapping of a Critical Region for Obesity and Hyperphagia [J].
D'Angelo, Carla S. ;
Kohl, Ilana ;
Varela, Monica Castro ;
de Castro, Claudia I. E. ;
Kim, Chong A. ;
Bertola, Debora R. ;
Lourenco, Charles M. ;
Koiffmann, Celia P. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A (01) :102-110
[4]   Monosomy 1p36 deletion syndrome [J].
Gajecka, Marzena ;
Mackay, Katherine L. ;
Shaffer, Lisa G. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2007, 145C (04) :346-356
[5]   Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome [J].
Heilstedt, HA ;
Ballif, BC ;
Howard, LA ;
Lewis, RA ;
Stal, S ;
Kashork, CD ;
Bacino, CA ;
Shapira, SK ;
Shaffer, LG .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (05) :1200-1212
[6]   CHROMOSOME-1P TERMINAL DELETION - REPORT OF NEW FINDINGS AND CONFIRMATION OF 2 CHARACTERISTIC PHENOTYPES [J].
KEPPLERNOREUIL, KM ;
CARROLL, AJ ;
FINLEY, WH ;
RUTLEDGE, SL .
JOURNAL OF MEDICAL GENETICS, 1995, 32 (08) :619-622
[7]   Growth charts for Down's syndrome from birth to 18 years of age [J].
Myrelid, Å ;
Gustafsson, J ;
Ollars, B ;
Annerén, G .
ARCHIVES OF DISEASE IN CHILDHOOD, 2002, 87 (02) :97-103
[8]  
Nagai T, 2000, AM J MED GENET, V95, P130, DOI 10.1002/1096-8628(20001113)95:2<130::AID-AJMG7>3.0.CO
[9]  
2-R
[10]   Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: A study of 5,380 cases [J].
Shao, Lina ;
Shaw, Chad A. ;
Lu, Xin-Yan ;
Sahoo, Trilochan ;
Bacino, Carlos A. ;
Lalani, Seema R. ;
Stankiewicz, Pawel ;
Yatsenko, Svetlana A. ;
Li, Yinfeng ;
Neill, Sarah ;
Pursley, Amber N. ;
Chinault, A. Craig ;
Patel, Ankita ;
Beaudet, Arthur L. ;
Lupski, James R. ;
Cheung, Sau W. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2008, 146A (17) :2242-2251