Results 31 to 40 of about 2,661 (168)
Prevalence of Epipteric Bones in Central Indian Adult Dry Skulls [PDF]
Background: A sutural bone is present at the pterion then it is called “Epipteric” or “Flower's bone”. They are frequently present in a variety of congenital disorders like hypothyroidism, cleidocranial dysostosis, progeria, rickets etc.
Ashwini R. Desai +3 more
doaj
Multidisciplinary management of cleidocranial dysplasia [PDF]
Background: Cleidocranial dysplasia (CCD), also known as cleidocranial dysostosis or osteodental dysplasia, is an autosomal dominant disorder caused by a microdeletion defect in chromosome 6p21.
Chalala, Chimène +3 more
core +1 more source
Critical View of Safety for Safe Laparoscopic Cholecystectomy [PDF]
Background: A sutural bone is present at the pterion then it is called “Epipteric” or “Flower's bone”. They are frequently present in a variety of congenital disorders like hypothyroidism, cleidocranial dysostosis, progeria, rickets etc.
Siddharth P. Dubhashi +2 more
doaj
ABSTRACT Objectives To develop a deep learning‐based framework to automate sector classification of unerupted maxillary canines (UMCs), assessing its accuracy and reliability compared to human ones. Material and Methods One thousand five hundred twenty‐eight UMCs from digital panoramic radiographs (PRs) were selected using data from the Dental ...
Marzio Galdi +7 more
wiley +1 more source
A Comparative Study of Pycnodysostosis, Cleidocranial Dysostosis, Osteopetrosis and Acro-osteolysis [PDF]
A radiological study of cases of pycnodysostosis, osteopetrosis, cleidocranial dysostosis and acro-osteolysis revealed an interwoven relationship as regards the X-ray findings with numerous identical signs that these conditions had in common.
Wolpowitz, A. +3 more
core
Cleidocranial dysplasia: A report of two cases
Cleidocranial dysplasia (CCD) is an autosomal dominant disorder that presents with skeletal dysplasia. It commonly presents with significant dental problems such as retention of multiple deciduous teeth, impaction or delay in eruption of permanent teeth,
D N Mehta, R V Vachhani, M B Patel
doaj +1 more source
Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders
Abstract Dental anomalies occur frequently in a number of genetic disorders and act as major signs in diagnosing these disorders. We present definitions of the most common dental signs and propose a classification usable as a diagnostic tool by dentists, clinical geneticists, and other health care providers.
Muriel de La Dure‐Molla +24 more
wiley +1 more source
Examples from the graphic library depicting morphologies of interparietal bones, ossicles at lambda, mendosal sutures, and intrasutural ossicles. Abstract Due to its complex ossification during development, the superior region of the human occipital bone is a frequent site of supernumerary bones known as interparietal bones.
Melissa D. Clarkson +4 more
wiley +1 more source
Marie-Sainton syndrome. Case reports
Marie-Sainton syndrome, also known as cleidocranial dysostosis, has a florid clinical picture dominated by changes in the clavicles and skull. Abnormalities in tooth eruption and dysmorphism are other distinctive features of this condition.
Reynaldo E. Delis Fernández +2 more
doaj
Phosphoinositide Metabolism: Biochemistry, Physiology and Genetic Disorders
ABSTRACT Phosphatidylinositol, a glycerophospholipid with a myo‐inositol head group, can form seven different phosphoinositides (PItds) by phosphorylation at inositol carbons 3, 4 and/or 5. Over 50 kinases and phosphatases participate in PItd metabolism, creating an interconnected PItd network that allows for precise temporal and spatial regulation of ...
Francis Rossignol +2 more
wiley +1 more source

