656 Congenital Myotonic Dystrophy: Smooth Muscle Involvement of the Urinary Tract in a 2 Year Old Child

被引：0
|
作者：
V Mundada
T Hildebrandt
机构：
[1] Paediatrics,
[2] Princess of Wales Hospital,undefined
来源：
Pediatric Research | 2010年 / 68卷
关键词：
D O I：
暂无
中图分类号：
学科分类号：
摘要：
We report a child with Congenital Myotonic Dystrophy (CDM1) who presented at the age of 28 months with marked smooth muscle involvement of the urinary tract Congenital Myotonic Dystrophy is a multi-system disorder affecting skeletal, smooth and cardiac muscles Smooth muscle involvement predominantly affects the gastrointestinal tract. Involvement of the urogenital smooth muscles is extremely rare and has so far only reported in adult cases There is little published on the effects of myotonia on the detrusor muscle.
引用
收藏
页码：335 / 336
页数：1
相关论文
共 50 条
  • [21] β2-microglobulin measurement with dried urine spots for congenital anomalies of the kidney and urinary tract screening in 3-year-old children
    Morohashi, Tamaki
    Wada, Naohiro
    Odaira, Sakiko
    Shimizu, Shoichi
    Takahashi, Shori
    Morioka, Ichiro
    PEDIATRICS INTERNATIONAL, 2022, 64 (01)
  • [22] Cardiac and skeletal muscle involvement in myotonic dystrophy type 2 (DM2):: A quantitative 31P-MRS and MRI study
    Schneider-Gold, C
    Beer, M
    Köstler, H
    Buchner, S
    Sandstede, J
    Hahn, D
    Toyka, KV
    MUSCLE & NERVE, 2004, 30 (05) : 636 - 644
  • [23] Rapid progressive subacute sclerosing panencephalitis in a 2-year-old child with congenital athyreosis
    Lackmann, GM
    Hannen, M
    Madjlessi, F
    Lenard, HG
    Schroten, H
    CLINICAL INFECTIOUS DISEASES, 2000, 31 (01) : 196 - 199
  • [24] Congenital Hepatic Fibrosis in a 2-Year-Old Child Presenting with Fever of Unknown Origin
    Penfold, Michael P.
    Annankra, Wentiirim B.
    Hull, Nathan C.
    Corredor, Margarita
    CASE REPORTS IN PEDIATRICS, 2023, 2023
  • [25] Heart involvement in type 1 and type 2 myotonic dystrophy. Insights from a 10-year follow-up study
    Fioravanti, F.
    Golzio, P. G.
    Carbone, M. L.
    Panarelli, A.
    Gagliardi, M.
    Mazzilli, S.
    Colopi, M.
    Ferraro, I
    Castagno, D.
    Giustetto, C.
    De Ferrari, G. M.
    EUROPEAN HEART JOURNAL, 2020, 41 : 3145 - 3145
  • [26] Death due to late-presenting congenital diaphragmatic hernia in a 2-year-old child
    Vandy, Frank C.
    Landrum, Jeffry E.
    Gerig, Nita R.
    Prahlow, Joseph A.
    AMERICAN JOURNAL OF FORENSIC MEDICINE AND PATHOLOGY, 2008, 29 (01): : 75 - 79
  • [27] Unique association of multiple endocrine neoplasia 2A and congenital anomalies of the kidney and urinary tract in a child with a RET mutation
    Wood, Olivia R.
    Else, Tobias
    Sampson, Matthew G.
    BMJ CASE REPORTS, 2019, 12 (08)
  • [28] Neovascular glaucoma from advanced coats disease as the initial manifestation of facioscapulohumeral dystrophy in a 2-year-old child
    Shields, Carol L.
    Zahler, Jonathan
    Falk, Naomi
    Furuta, Minoru
    Eagle, Ralph C., Jr.
    Espinosa, Luis E. Bello
    Fischer, Philip R.
    Shields, Jerry A.
    ARCHIVES OF OPHTHALMOLOGY, 2007, 125 (06) : 840 - 842
  • [29] Right ventricular outflow tract resection for treatment of refractory ventricular tachycardia in a 2-year-old child
    Kanaan, S
    Shamsuddin, K
    Silka, M
    Wells, W
    JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2005, 130 (03): : 948 - +
  • [30] URINARY-EXCRETION OF THYMINE AND URACIL IN A 2-YEAR-OLD CHILD WITH A MALIGNANT-TUMOR OF THE BRAIN
    BERGLUND, G
    GRETER, J
    LINDSTEDT, S
    STEEN, G
    WALDENSTROM, J
    WASS, U
    CLINICAL CHEMISTRY, 1979, 25 (07) : 1325 - 1328
12345