Results 21 to 30 of about 5,692 (182)

Metopic synostosis [PDF]

open access: yesChild's Nervous System, 2012
Premature closure of the metopic suture results in a growth restriction of the frontal bones, which leads to a skull malformation known as trigonocephaly. Over the course of recent decades, its incidence has been rising, currently making it the second most common type of craniosynostosis.
openaire   +2 more sources

Complete Maxillo-Mandibular Syngnathia in a Newborn with Multiple Congenital Malformations

open access: yesPediatrics and Neonatology, 2016
Syngnathia is an extremely rare condition involving congenital fusion of the maxilla with the mandible. Clinical presentations vary from simple mucosal bands (synechiae) to complete bony fusion (synostosis).
M. Broome   +5 more
doaj   +1 more source

Congenital Humeroradial Synostosis: A Case Report [PDF]

open access: yesMalaysian Orthopaedic Journal, 2012
We present here a unique case of humeroradial synostosis. These anomalies are due to longitudinal failure of differentiation. Approximately 150 cases of humeroradial synostosis have been reported worldwide, the majority of which are familial in nature or
Sandeep Nema   +3 more
doaj   +1 more source

Congenital radioulnar synostosis presenting in adulthood - a case report

open access: yesThe Pan African Medical Journal, 2020
Congenital radioulnar synostosis is a rare developmental skeletal malformation of the upper limb, characterized by the fusion of the proximal ends of the radius and ulna from birth. The failure of prenatal longitudinal segmentation of the adjacent radius
Mohammed Hamid Karrar Alsharif   +6 more
doaj   +1 more source

QS3: Influence Of Nonsyndromic Bicoronal Synostosis And Syndromic Influences On And Periorbital Malformation

open access: yesPlastic and Reconstructive Surgery, Global Open, 2021
Background Oculo-orbital disproportion in patients with craniosynostosis have similarities and dissimilarities between syndromic and nonsyndromic cases. We hypothesize these two conditions have specific individual influences as it relates to development ...
Xiaona Lu, MD, PhD   +4 more
doaj   +1 more source

SURGICAL TREATMENT OF METACARPAL SYNOSTOSIS IN CHILDREN

open access: yesTravmatologiâ i Ortopediâ Rossii, 2012
Objective: to develop the surgical treatment of patients with congenital metacarpal synostosis. Material and methods. 65 operations were performed in 58 children. with congenital metacarpal synostosis.
A. V. Zaletina
doaj   +1 more source

MEDICAL IMAGING AND 3D RECONSTRUCTION FOR OBTAINING THE GEOMETRICAL AND PHYSICAL MODEL OF A CONGENITAL BILATERAL RADIO-ULNAR SYNOSTOSIS [PDF]

open access: yesApplied Computer Science, 2018
The paper presents results of a 3D reconstruction of a congenital bilateral radio-ulnar synostosis. Basics of anatomy and biomechanical analysis of the elbow joint were introduced.
Robert KARPIŃSKI   +2 more
doaj   +1 more source

Clinical and Cytogenomic Characterization of Three Patients With Distal 1q43q44 Deletion: Twin Sisters With a de novo Deletion and a Patient With der(1)t(1;21)(q43;q22.3)mat

open access: yesJournal of Clinical Laboratory Analysis, EarlyView.
Distal 1q43q44 deletions lead to a consistent neurodevelopmental phenotype characterized by microcephaly, corpus callosum abnormalities, and developmental delay. Despite differences in genomic architecture, overlapping deletions affecting dosage‐sensitive genes such as AKT3, HNRNPU, and ZBTB18 define the core phenotype.
Ma. Guadalupe Domínguez‐Quezada   +6 more
wiley   +1 more source

Painful Locking Elbow in a Child with Congenital Proximal Radioulnar Synostosis

open access: yesJournal of Hand Surgery Global Online, 2019
Painful snapping or locking in the elbow is an uncommon presentation that has been observed in children with proximal radioulnar synostosis. Only a few cases have been reported in the English language literature.
Nezar B. Hamdi, MD, SBOS   +3 more
doaj   +1 more source

Cortical Thickness in Crouzon–Pfeiffer Syndrome: Findings in Relation to Primary Cranial Vault Expansion

open access: yesPlastic and Reconstructive Surgery, Global Open, 2020
Background:. Episodes of intracranial hypertension are associated with reductions in cerebral cortical thickness (CT) in syndromic craniosynostosis. Here we focus on Crouzon–Pfeiffer syndrome patients to measure CT and evaluate associations with type of ...
Alexander T. Wilson, BS   +7 more
doaj   +1 more source

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