z-logo
Premium
Prenatal findings in generalized amyoplasia
Author(s) -
Sepulveda Waldo,
Stagiannis Konstantinos D.,
Cox Phillip M.,
Wigglesworth Jonathan S.,
Fisk Nicholas M.
Publication year - 1995
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.1970150712
Subject(s) - polyhydramnios , maldevelopment , muscle contracture , arthrogryposis , autopsy , medicine , prenatal diagnosis , fetus , anatomy , obstetrics , pathology , pregnancy , biology , genetics
Amyoplasia is a rare, sporadic condition characterized by different degrees of maldevelopment of the skeletal muscles, which are replaced by fibrous and fatty tissue. In this report, we present a case of generalized amyoplasia presenting at 19 weeks' gestation. The most striking finding was the absence of fetal movements, resulting in severe multiple congenital contractures, hydrops, and polyhydramnios. At autopsy, histological examination of the skeletal muscle showed small groups of poorly developed fibres within areas of fat. This report suggests that generalized amyoplasia could be a common cause of severe forms of multiple congenital contractures, but is probably underdiagnosed at post‐mortem because of inadequate examination of muscles. Definitive diagnosis is important in determining the risks of recurrence in these cases.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom