Unusual fetal movement in congenital myotonic dystrophy

Chaur Dong Hsu; Terry I. F Eng; Thomas O. Crawford; Timothy R.B. Johnson

doi:10.1159/000263825

Unusual fetal movement in congenital myotonic dystrophy

Chaur Dong Hsu
, Terry I. F Eng
, Thomas O. Crawford
, Timothy R.B. Johnson

Research output: Contribution to journal › Article › peer-review

12 Scopus citations

Abstract

Congenital myotonic dystrophy is the most extreme and early expression of a multisystem autosomal dominant disorder. Decreased fetal and infantile movement is a defining feature. We report a case of congenital myotonic dystrophy with an unusual pattern of persistent repetitive fetal movements detected by a Doppler fetal movement detector.

Original language	English (US)
Pages (from-to)	200-202
Number of pages	3
Journal	Fetal Diagnosis and Therapy
Volume	8
Issue number	3
DOIs	https://doi.org/10.1159/000263825
State	Published - 1993
Externally published	Yes

Keywords

Congenital myotonic dystrophy
Femur fracture
Fetal movement

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Embryology
Radiology Nuclear Medicine and imaging
Obstetrics and Gynecology

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10.1159/000263825

Cite this

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title = "Unusual fetal movement in congenital myotonic dystrophy",

abstract = "Congenital myotonic dystrophy is the most extreme and early expression of a multisystem autosomal dominant disorder. Decreased fetal and infantile movement is a defining feature. We report a case of congenital myotonic dystrophy with an unusual pattern of persistent repetitive fetal movements detected by a Doppler fetal movement detector.",

keywords = "Congenital myotonic dystrophy, Femur fracture, Fetal movement",

author = "Hsu, \{Chaur Dong\} and \{F Eng\}, \{Terry I.\} and Crawford, \{Thomas O.\} and Johnson, \{Timothy R.B.\}",

year = "1993",

doi = "10.1159/000263825",

language = "English (US)",

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T1 - Unusual fetal movement in congenital myotonic dystrophy

AU - Hsu, Chaur Dong

AU - F Eng, Terry I.

AU - Crawford, Thomas O.

AU - Johnson, Timothy R.B.

PY - 1993

Y1 - 1993

N2 - Congenital myotonic dystrophy is the most extreme and early expression of a multisystem autosomal dominant disorder. Decreased fetal and infantile movement is a defining feature. We report a case of congenital myotonic dystrophy with an unusual pattern of persistent repetitive fetal movements detected by a Doppler fetal movement detector.

AB - Congenital myotonic dystrophy is the most extreme and early expression of a multisystem autosomal dominant disorder. Decreased fetal and infantile movement is a defining feature. We report a case of congenital myotonic dystrophy with an unusual pattern of persistent repetitive fetal movements detected by a Doppler fetal movement detector.

KW - Congenital myotonic dystrophy

KW - Femur fracture

KW - Fetal movement

UR - https://www.scopus.com/pages/publications/0027488706

UR - https://www.scopus.com/pages/publications/0027488706#tab=citedBy

U2 - 10.1159/000263825

DO - 10.1159/000263825

M3 - Article

C2 - 8240694

AN - SCOPUS:0027488706

SN - 1015-3837

VL - 8

SP - 200

EP - 202

JO - Fetal Diagnosis and Therapy

JF - Fetal Diagnosis and Therapy

IS - 3

ER -

Unusual fetal movement in congenital myotonic dystrophy

Abstract

Keywords

ASJC Scopus subject areas

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