Results 91 to 100 of about 4,694 (215)

Freeman-Sheldon Syndrome: A Rare Case Report with Dental Perspective

open access: yesPrague Medical Report
Freeman-Sheldon syndrome is a rare form of multiple congenital contracture syndromes (arthrogryposes) and is the most severe form of distal arthrogryposis. The main skeletal malformations include camptodactyly with ulnar deviation and talipes equinovarus
Sahil Mustafa Kidwai   +3 more
doaj   +1 more source

Expanding the Genotype–Phenotype Correlation of Marden–Walker Syndrome due to PIEZO2 Gene Variants: A Case Report From Brazil

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 5, Page 1156-1161, May 2026.
ABSTRACT Marden–Walker syndrome (MWS; OMIM 248700) is an extremely rare congenital disorder characterized by multiple joint contractures, craniofacial dysmorphism, neurological abnormalities, and multisystem involvement. Although historically diagnosed on clinical grounds, only a few cases have been molecularly confirmed.
Guilherme Sotto Battiston   +35 more
wiley   +1 more source

A Four-year Review of Delayed Initial Treatment of Patients with Congenital Talipes equinovarus in a General Hospital [PDF]

open access: yes, 2015
Congenital Talipes Equinovarus (CTEV), or club foot, is a common congenital orthopaedic abnormality of the foot, which is easily diagnosed but difficult to treat perfectly.
Yoyos DI
core   +1 more source

Larsen syndrome

open access: yesBangabandhu Sheikh Mujib Medical University Journal, 2016
Larsen syndrome is a rare inherited disorder characterized by congenital dislocation of multiple joints along with other anomalies of heart, face, hands and bones. Larsen syndrome was first described in 1950 by Larsen, Schottstaedt and Bost.
Mohammed Mahbubul Islam   +5 more
doaj   +1 more source

Frequency of hospitalization in patients diagnosed with congenital talipes equinovarus (CTEV) [PDF]

open access: yes, 2015
Introduction. Congenital talipes equinovarus (CTEV), also called clubfoot is the second after congenital dysplasia of the hip (CDH) most frequently occurring congenital limb defect. In Europe the deformity affects 1-2 newborns in 1000 live births.
Piotr Książek   +9 more
core   +1 more source

A Literature Review of Non-Surgical Intervention for the Treatment of Idiopathic Talipes Equinovarus: A Podiatric Perspective [PDF]

open access: yes, 2010
This article aims to discuss the current surgical and non-surgical interventions in the treatment of idiopathic talipes equinovarus. It examines the literature from 1964 to the present day and includes a detailed anatomical description of the condition ...
McGroggan, J   +3 more
core   +1 more source

Severe Nonketotic Hyperglycinemia in Twins Caused by GLDC Variants: The Importance of Accurate Prenatal Variant Interpretation, Counseling, and VUS Disclosure

open access: yes
Prenatal Diagnosis, Volume 46, Issue 8, Page 1294-1297, July 2026.
Christopher Connolly   +6 more
wiley   +1 more source

Evaluation of Ponseti method in correction of congenital talipes equinovarus [PDF]

open access: yes, 2018
<p class="abstract"><strong>Background:</strong> Congenital idiopathic clubfoot is a complex foot deformity often requires many months of treatment and frequently resulted in incomplete or defective correction by older methods ...
Shinde, Gopal M.   +9 more
core   +1 more source

Turco’s Postero-Medial Release for Congenital Talipes Equino-Varus

open access: yesGomal Journal of Medical Sciences, 2004
Background: Talipes equino-varus is the most common congenital orthopaedic anomaly. There are various methods for its management. This study was conducted to determine the efficacy of Turco’s one stage postero-medial release in children with congenital ...
Shakir Hussain   +4 more
doaj  

Study of congenital talipes equinovarus cases and its radiological correlation

open access: yesNational Journal of Clinical Anatomy, 2013
Background and aims : congenital talipes equinovarus (CTEV) or club foot is one of the most common congenital orthopaedic anomalies and is increasing day by day with the growing millions of this country.
Prabahita Baruah   +2 more
doaj   +1 more source

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