A maternally transmitted lethal neonatal progeroid syndrome with prominent genitourinary and gastrointestinal features

被引:8
作者
Delatycki, MB
Cleary, MA
Bankier, A
McDougall, PN
Ahluwalia, JS
Chow, CW
CookeYarborough, CM
机构
[1] ROYAL CHILDRENS HOSP,DEPT PATHOL,PARKVILLE,VIC 3052,AUSTRALIA
[2] ROYAL CHILDRENS HOSP,DEPT NEONATOL,PARKVILLE,VIC 3052,AUSTRALIA
关键词
progeroid; pseudo-obstruction; mitochondria;
D O I
10.1136/jmg.34.6.520
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Twin brothers and their maternal uncle with a previously undescribed neonatal progeroid syndrome are presented. In addition to progeroid features, they had pseudo-obstruction of the urinary and gastrointestinal tracts, severe leucocytosis, liver dysfunction, and low complex III and IV in muscle but not in liver. Previously described neonatal progeroid syndromes and syndromes featuring pseudoobstruction are discussed. The two most likely aetiological mechanisms are an X linked single gene disorder or a mitochondrial disorder. The evidence for these possibilities is presented.
引用
收藏
页码:520 / 524
页数:5
相关论文
共 15 条
[1]  
Auricchio A, 1996, AM J HUM GENET, V58, P743
[2]  
BITOUN P, 1995, CLIN DYSMORPHOL, V4, P239
[3]  
DEMARTINVILLE B, 1980, ARCH FR PEDIATR, V37, P679
[4]   THE WIEDEMANN-RAUTENSTRAUCH OR NEONATAL PROGEROID SYNDROME - REPORT OF A PATIENT WITH CONSANGUINEOUS PARENTS [J].
DEVOS, EA ;
LEROY, JG ;
FRIJNS, JP ;
VANDENBERGHE, H .
EUROPEAN JOURNAL OF PEDIATRICS, 1981, 136 (03) :245-248
[5]   NEONATAL PROGEROID SYNDROME - MORE THAN ONE DISEASE [J].
HAGADORN, JI ;
WILSON, WG ;
HOGGE, WA ;
CALLICOTT, JH ;
BEALE, EF .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1990, 35 (01) :91-94
[6]  
HARRIS DJ, 1976, CLIN GENET, V9, P479
[7]   MULTIPLE MITOCHONDRIAL-DNA DELETIONS IN MYO-NEURO-GASTROINTESTINAL ENCEPHALOPATHY SYNDROME [J].
JOHNS, DR ;
THRELKELD, AB ;
MILLER, NR ;
HURKO, O .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1993, 115 (01) :108-109
[8]   THE WIEDEMANN-RAUTENSTRAUCH OR NEONATAL PROGEROID SYNDROME NEUROPATHOLOGICAL STUDY OF A CASE [J].
MARTIN, JJ ;
CEUTERICK, CM ;
LEROY, JG ;
DEVOS, EA ;
ROELENS, JG .
NEUROPEDIATRICS, 1984, 15 (01) :43-48
[9]   Leigh syndrome: Clinical features and biochemical and DNA abnormalities [J].
Rahman, S ;
Blok, RB ;
Dahl, HHM ;
Danks, DM ;
Kirby, DM ;
Chow, CW ;
Christodoulou, J ;
Thorburn, DR .
ANNALS OF NEUROLOGY, 1996, 39 (03) :343-351
[10]   PROGERIA - CELL-CULTURE STUDY AND CLINICAL REPORT OF FAMILIAL INCIDENCE [J].
RAUTENSTRAUCH, T ;
SNIGULA, F ;
KRIEG, T ;
GAY, S ;
MULLER, PK .
EUROPEAN JOURNAL OF PEDIATRICS, 1977, 124 (02) :101-111