Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairment

被引:46
作者
Anderlid, BM
Schoumans, J
Hallqvist, Å
Ståhl, Y
Wallin, A
Blennow, E
Nordenskjöld, M
机构
[1] Karolinska Hosp, Karolinska Inst, Dept Mol Med, Clin Genet Unit, SE-17176 Stockholm, Sweden
[2] Karolinska Hosp, Astrid Lindgrens Childrens Hosp, Dept Neuropediat, SE-17176 Stockholm, Sweden
[3] St Eriks Eye Hosp, Danderyd Hosp, Dept Pediat Ophtalmol & Strabismus, Stockholm, Sweden
关键词
6p; deletion; subtelomeric; cryptic; language impairment; FISH;
D O I
10.1038/sj.ejhg.5200907
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several cases with microscopically visible, terminal 6p deletions have been described, and a distinct clinical phenotype has emerged, including developmental delay, congenital heart malformations, ocular abnormalities, hearing loss and a characteristic facial appearance. We report a patient with a submicroscopic 6p deletion, detected by subtelomeric screening using fluorescence in situ hybridisation. This girl presented with typical facial dysmorphic features, hearing impairment, malformation of the anterior eye segment, an ASD and severe language impairment. However, her cognitive functions were within the normal range. Detailed FISH analysis with 20 BAC probes covering the distal 6p25 region estimated the size of the terminal deletion to 2.1 Mb, and thus this case narrows down the critical region for the 6p phenotype. The forkhead transcription factor gene FOXC1, involved in a spectrum of anterior eye chamber disorders, is deleted in this patient, together with several characterised and putative genes with yet unknown function.
引用
收藏
页码:89 / 92
页数:4
相关论文
共 20 条
[1]  
Aitola M, 2000, DEV DYNAM, V218, P136, DOI 10.1002/(SICI)1097-0177(200005)218:1<136::AID-DVDY12>3.0.CO
[2]  
2-U
[3]   Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia [J].
Clifton-Bligh, RJ ;
Wentworth, JM ;
Heinz, P ;
Crisp, MS ;
John, R ;
Lazarus, JH ;
Ludgate, M ;
Chatterjee, VK .
NATURE GENETICS, 1998, 19 (04) :399-401
[4]   The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome [J].
Crisponi, L ;
Deiana, M ;
Loi, A ;
Chiappe, F ;
Uda, M ;
Amati, P ;
Bisceglia, L ;
Zelante, L ;
Nagaraja, R ;
Porcu, S ;
Ristaldi, MS ;
Marzella, R ;
Rocchi, M ;
Nicolino, M ;
Lienhardt-Roussie, A ;
Nivelon, A ;
Verloes, A ;
Schlessinger, D ;
Gasparini, P ;
Bonneau, D ;
Cao, A ;
Pilia, G .
NATURE GENETICS, 2001, 27 (02) :159-166
[5]   A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome [J].
Davies, AF ;
Olavesen, MG ;
Stephens, RJ ;
Davidson, R ;
Delneste, D ;
VanRegemorter, N ;
Vamos, E ;
Flinter, F ;
Abusaad, I ;
Ragoussis, J .
HUMAN GENETICS, 1996, 98 (04) :454-459
[6]   Delineation of two distinct 6p deletion syndromes [J].
Davies, AF ;
Mirza, G ;
Sekhon, G ;
Turnpenny, P ;
Leroy, F ;
Speleman, F ;
Law, C ;
van Regemorter, N ;
Vamos, E ;
Flinter, F ;
Ragoussis, J .
HUMAN GENETICS, 1999, 104 (01) :64-72
[7]   Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome [J].
Fang, JM ;
Dagenais, SL ;
Erickson, RP ;
Arlt, MF ;
Glynn, MW ;
Gorski, JL ;
Seaver, LH ;
Glover, TW .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (06) :1382-1388
[8]   Localisation of a gene implicated in a severe speech and language disorder [J].
Fisher, SE ;
Vargha-Khadem, F ;
Watkins, KE ;
Monaco, AP ;
Pembrey, ME .
NATURE GENETICS, 1998, 18 (02) :168-170
[9]   Cloning of human lymphocyte-specific interferon regulatory factor (hLSIRF/hIRF4) and mapping of the gene to 6p23-p25 [J].
Grossman, A ;
Mittrucker, HW ;
Nicholl, J ;
Suzuki, A ;
Chung, S ;
Antonio, L ;
Suggs, S ;
Sutherland, GR ;
Siderovski, DP ;
Mak, TW .
GENOMICS, 1996, 37 (02) :229-233
[10]   Five years on the wings of fork head [J].
Kaufmann, E ;
Knochel, W .
MECHANISMS OF DEVELOPMENT, 1996, 57 (01) :3-20