๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Morphology of the orbital region in adults following the cleft lip/palate repair in childhood

โœ Scribed by Leslie G. Farkas; William K. Lindsay; Meindert B. Vanderby


Publisher
John Wiley and Sons
Year
1972
Tongue
English
Weight
652 KB
Volume
37
Category
Article
ISSN
0002-9483

No coin nor oath required. For personal study only.

โœฆ Synopsis


Four measurements and two qualitative signs related to the orbits of 145 adult Caucasian cleft liplpalate patients operated on in childhood were compared with similar data on 100 normal Caucasian Canadians. The average interorbital distance in male patients with unilateral and bilateral cleft liplpalate was greater than i n controls, while the interorbital distance i n both male and female patients with isolated cleft palate was the same as that in controls. A hypertelorism increased interorbital distance of greater than 2 S.D. above the normal was recorded in 10 cleft patients out of 145, the maximum in male cleft patients being 48 mm and i n female cleft patients 38 mm.

Orbital eye fissure length asymmetry was seen only in the cleft study group while a dislocation of the eye fissure levels i n the frontal plane was found both in patients with clefts and in controls. No direct relationship was found between the extent of the cleft and the incidence of hypertelorism, nor between the site of the cleft and eye fissure asymmetry in unilateral cleft lip/palate patients.

The epicanthic fold was significantly more frequent in cleft lip/palate patients (28/145) than i n controls (lO/lOO). Anti-mongoloid eye fissure type was recorded only in patients with cleft but mongoloid eye fissure was present both in patients with clefts and controls.


๐Ÿ“œ SIMILAR VOLUMES


Investigations of the genomic region tha
โœ Diana M. Juriloff; Muriel J. Harris; Sarah L. Dewell; Carolyn J. Brown; Dixie L. ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 261 KB ๐Ÿ‘ 2 views

## Abstract ## BACKGROUND Human nonsyndromic cleft lip and palate, CL(P), is genetically complex, with one contributing gene on chromosome 17q. A potentially homologous gene, __clf1__ on distal chromosome 11, is part of the digenic cause of the 10โ€“30% CL(P) in the A/WySn mouse strain. Here we repo

Association between genetic variants of
โœ Adrianna Mostowska; Kamil K. Hozyasz; Piotr Wojcicki; Barbara Biedziak; Patrycja ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 103 KB ๐Ÿ‘ 2 views

## Abstract ## BACKGROUND Cleft lip with or without cleft palate (CL/P) is one of the most common craniofacial malformations, with a complex and multifactorial etiology. Because of the genetic heterogeneity of facial clefts, the aim of this study was to investigate the contribution of previously r