Skeletal malformations in fetuses with Meckel syndrome.

Bidragets oversatte titel: Skeletal malformations in fetuses with Meckel syndrome.

K W Kjaer, B Fischer Hansen, J W Keeling, I Kjaer

10 Citationer (Scopus)

Abstract

In six fetuses with Meckel syndrome (gestational age 16-23 weeks, crown-rump length 130-170 mm) the skeleton was examined as part of the autopsy procedure using whole body radiography and special radiographic techniques. In the upper and lower limbs we found similar types of polydactyly. We noted four types, based on the number and morphology of metacarpals and metatarsals. In the individual fetus there was more often similarity in the pattern of malformation in the two hands or in the two feet than there was between the pattern of malformation seen in the hands and that seen in the feet. Only one foot was normal. Malformations of the cranial base (the basilar part of the occipital bone or the postsphenoid bone) occurred in five cases, and the vertebral bodies in the lumbar region of the spine were malformed (cleft) in three cases. It is proposed that a skeletal analysis be included in the future evaluation of phenotypes in Meckel syndrome.
Bidragets oversatte titelSkeletal malformations in fetuses with Meckel syndrome.
OriginalsprogEngelsk
TidsskriftAmerican Journal of Medical Genetics. Part A
Vol/bind84
Udgave nummer5
Sider (fra-til)469-475
Antal sider7
ISSN1552-4825
StatusUdgivet - 1999

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