𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Craniofacial structure in Marfan syndrome: A cephalometric study

✍ Scribed by De Coster, Peter ;Pauw, Guy De ;Martens, Luc ;De Paepe, Anne

Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
191 KB
Volume
131A
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Craniofacial structure in diastrophic dy
Craniofacial structure in diastrophic dysplasiaβ€”a cephalometric study
✍ Karlstedt, Eva; Kaitila, Ilkka; Pirinen, Sinikka πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 94 KB πŸ‘ 2 views

Diastrophic dysplasia (DTD) is a well characterized, recessively inherited osteochondrodysplasia. Forty-eight patients with DTD were studied for craniofacial characteristics. Of these patients, 58% had cleft palate. A cephalometric analysis based on lateral cephalograms was performed. We observed a

Craniofacial morphology in patients with
Craniofacial morphology in patients with hypophosphatemic rickets: A cephalometric study focusing on differences between bone of cartilaginous and intramembranous origin
✍ Hans GjΓΈrup; Inger KjΓ¦r; Liselotte Sonnesen; Dorte Haubek; Signe Sparre Beck-Nie πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 237 KB

## Abstract Hypophosphatemic rickets (HR) are diseases characterized by deficient mineralization of bone due to abnormal renal wasting of phosphate. Deformation of bony structures of cartilaginous origin has been described as a major characteristic in patients with HR, but little is known about the

Primary trabeculodysgenesis in associati
Primary trabeculodysgenesis in association with neonatal Marfan syndrome
✍ Charlotte M. Whitelaw; Samira Anwar; Lesley C. AdΓ¨s; Glen A. Gole; James E. Elde πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 167 KB

## Abstract We present the clinical and ophthalmological findings in two infants with neonatal Marfan syndrome (nMFS) and primary trabeculodysgenesis (PT). Fibrillin 1 (FBN1) mutations were confirmed in both cases. Numerous eye anomalies have been recognized in infants with nMFS, but PT has not bee