Successful pregnancy in a woman with glycogen storage disease type III

Australian and New Zealand Journal of Obstetrics and Gynaecology

Volumn 46, Issue 2, 2006, Pages 168-169

  Bhatti, Shazia ^a,c   Parry, Emma ^b  

^a NATIONAL WOMEN S HOSPITAL   (New Zealand)

^b UNIVERSITY OF AUCKLAND   (New Zealand)

^c ADDENBROOKE S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE AMINOTRANSFERASE; ASPARTATE AMINOTRANSFERASE; CREATINE KINASE; GLUCOSE;

ADULT; AMNIOCENTESIS; ARTICLE; BODY MASS; CASE REPORT; CESAREAN SECTION; DISEASE SEVERITY; FEMALE; FETUS GROWTH; GENETIC COUNSELING; GESTATION PERIOD; GLUCOSE BLOOD LEVEL; GLYCOGEN STORAGE DISEASE TYPE 3; HIGH RISK POPULATION; HUMAN; HYPOGLYCEMIA; LABORATORY DIAGNOSIS; LACTIC ACIDOSIS; PREGNANCY; PRENATAL CARE; PRIORITY JOURNAL;

ADULT; FEMALE; FOLLOW-UP STUDIES; GESTATIONAL AGE; GLYCOGEN STORAGE DISEASE TYPE III; HUMANS; LABOR, INDUCED; MATERNAL AGE; MONITORING, PHYSIOLOGIC; PREGNANCY; PREGNANCY COMPLICATIONS; PREGNANCY OUTCOME; PREGNANCY, HIGH-RISK; RISK ASSESSMENT;

EID: 33645367281     PISSN: 00048666     EISSN: 1479828X     Source Type: Journal    
DOI: 10.1111/j.1479-828X.2006.00549.x     Document Type: Article

References (8)

1. Coleman RA, Winter HS, Wolf B, Chen YT. Glycogen debranching enzyme deficiency: Long term study of serum enzyme activities and clinical features. J Inherit Met Dis 1992; 15: 869-881.
2. Coleman RA, Winter HS, Wolf B, Gilchrist JM, Chen YT. Glycogen storage disease type III (glycogen debranching enzyme deficiency): Correlation of biochemical defects with myopathy and cardiomyopathy. Ann Int Med 1992; 116: 896-900.
3. Yang BZ, Ding JH, Brown BI, Chen YT. Definitive prenatal diagnosis for type III glycogen storage disease. Am J Hum Genet 1990; 47: 735-739.
4. Lee PJ, Patel A, Hindmarsh PC, Mowat AP, Leonard JV. The prevalence of polycystic ovaries in the hepatic glycogen storage diseases: Its association with hyperinsulinism. Clin Endocrinol 1995; 42: 601-666.
5. Watts C, Gain K, Malthus R. Blood glucose of mother and fetus late pregnancy of rats with glycogen storage disorder. Biol Neonate 1982; 41: 204-208.
6. Shen J, Liu HM, McConkie-Rossell A, Chen YT. Prenatal diagnosis and carrier detection for glycogen storage disease type III using polymorphic DNA markers. Prenat Diagn 998: 61-64.
7. Mendoza A, Fisher NC, Duckett J et al. Successful pregnancy in a patient with type lll glycogen storage disease managed with cornstarch supplements. Br J Obstet Gynaecol 1998; 105: 677-680.
8. Confino E, Pauzner D, Lidor A, Yedwab G, David M. Pregnancy associated with amylo-1,6-glucosidase deficiency (Forbe's disease). Case report. Br J Obstet Gynaecol 1984; 91: 494-497.