𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Keutel syndrome with overlapping features of cutis laxa: A new variant

✍ Scribed by Arti Nanda; Jehoram T. Anim; Meshal Al-Gareeb; Qasem A. Alsaleh


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
207 KB
Volume
140A
Category
Article
ISSN
1552-4825

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Syndrome of congenital cutis laxa with l
✍ Oğur, GΓΆnΓΌl ;YΓΌksel-Apak, Memnune ;Demiryont, Misten πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 631 KB

## Abstract Congenital cutis laxa with ligamentous laxity and delayed development has recently been defined as a distinct entity of autosomal recessive inheritance. Here we report on 2 new cases of this syndrome. With severe manifestations in the male, X‐linked dominant inheritance is discussed. Re

A boy with developmental delay, malforma
✍ Armstrong, Linlea ;Jimenez, Carmencita ;Hunter, Alasdair G.W. πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 296 KB πŸ‘ 1 views

## Abstract We report a 7.5‐year‐old boy with loose translucent skin, aortic dilatation, hyperextensible veins, recurrent respiratory problems, pectus excavatum, arthralgias, lax joints, mild epiphyseal dysplasia, and umbilical and inguinal hernias. He also has developmental delay, progressive bila