Menorrhagia in Patients With Type I Glycogen Storage Disease

被引:7
|
作者
Austin, Stephanie L.
El-Gharbawy, Areeg H.
Kasturi, Vellore G.
James, Andra
Kishnani, Priya S.
机构
[1] Duke Univ, Med Ctr, Dept Pediat, Div Med Genet, Durham, NC 27710 USA
[2] Univ Pittsburgh, Med Ctr, Pittsburgh, PA USA
[3] Univ Virginia, Sch Med, Dept Obstet & Gynecol, Charlottesville, VA 22908 USA
来源
OBSTETRICS AND GYNECOLOGY | 2013年 / 122卷 / 06期
关键词
ENDOMETRIAL ABLATION; CLINICAL-COURSE; BLOOD-LOSS; WOMEN; MANAGEMENT; PREVALENCE; PREGNANCY; RISK;
D O I
10.1097/01.AOG.0000435451.86108.82
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: To evaluate menorrhagia in a cohort of women with glycogen storage disease type I because it appears to be an under-recognized problem in females of reproductive age. METHODS: A retrospective chart review was performed on 13 menstruating patients with glycogen storage disease type I (age 23-48 years) for a diagnosis of menorrhagia. RESULTS: Nine (69%) (confidence interval 0.39-0.91) women had development of menorrhagia. Median hemoglobin values in these patients were generally low (range 9.5-12.85 g/dL) but not different from those of the non-menorrhagia group (hemoglobin range 9.55-11.0 g/dL) with glycogen storage disease type I. Four patients with menorrhagia required hospitalization or emergency department visits for treatment of menorrhagia. Two of the four patients hospitalized required blood transfusion, with an additional patient requiring a transfusion during pregnancy. Eight patients (89%) either were recommended to have or required medical or surgical treatment of their menorrhagia. CONCLUSION: Glycogen storage disease type I is associated with menorrhagia. The evaluation should include assessment of coagulation functions and referral to a gynecologist, hematologist, or both, because bleeding diathesis and polycystic ovary syndrome are common in patients with glycogen storage disease type I.
引用
收藏
页码:1246 / 1254
页数:9
相关论文
共 50 条
  • [31] Steno-occlusive cerebral arteriopathy in patients with glycogen storage disease type I
    Hong, Yuehui
    Yuan, Yuheng
    Shu, Shi
    Hou, Bo
    Dai, Yi
    Ni, Jun
    Feng, Feng
    Qiu, Zhengqing
    Peng, Bin
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2020, 91 (04): : 434 - 435
  • [32] Dietary dilemmas in the management of glycogen storage disease type I
    Bhattacharya, Kaustuv
    JOURNAL OF INHERITED METABOLIC DISEASE, 2011, 34 (03) : 621 - 629
  • [33] Glycogen storage disease type I: pathophysiology of liver adenomas
    Philip J Lee
    European Journal of Pediatrics, 2002, 161 (1) : S46 - S49
  • [34] GLYCOGEN-STORAGE-DISEASE TYPE-I - PREFACE
    MOSES, SW
    SHIN, YS
    SMIT, GPA
    ULLRICH, K
    EUROPEAN JOURNAL OF PEDIATRICS, 1993, 152 : S1 - S1
  • [35] Glycogen storage disease type I in Tunisia: An epidemiological analysis
    Ben Chehida, A.
    Tebib, N.
    Cherif, W.
    Ben Turkia, H.
    Abdelmoula, S.
    Azzouz, H.
    Ben Dridi, M. F.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2008, 31 : S199 - S204
  • [36] MOLECULAR DIAGNOSIS OF GLYCOGEN STORAGE DISEASE TYPE I: A REVIEW
    Beyzaei, Zahra
    Geramizadeh, Bita
    EXCLI JOURNAL, 2019, 18 : 30 - 46
  • [37] PLATELET DYSFUNCTION IN GLYCOGEN STORAGE-DISEASE TYPE I
    CZAPEK, EE
    SALZMAN, EW
    DEYKIN, D
    FEDERATION PROCEEDINGS, 1972, 31 (02) : A242 - &
  • [38] NEUROMUSCULAR ALTERATIONS IN GLYCOGEN STORAGE DISEASE TYPE I AND IIIA
    Sentner, C. P.
    van der Hoeven, J. H.
    Maurits, N. M.
    Verbeek, R. J.
    Smit, G. P. A.
    Sival, D. A.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2012, 35 : S79 - S79
  • [39] Psychosocial functioning in youth with glycogen storage disease type I
    Storch, Eric
    Keeley, Mary
    Merlo, Lisa
    Jacob, Marni
    Correia, Catherine
    Weinstein, David
    JOURNAL OF PEDIATRIC PSYCHOLOGY, 2008, 33 (07) : 728 - 738
  • [40] GLYCOGEN-STORAGE-DISEASE TYPE-I - REPLY
    SCHWENK, WF
    HAYMOND, MW
    NEW ENGLAND JOURNAL OF MEDICINE, 1986, 315 (08): : 521 - 521