Results 81 to 90 of about 265,498 (210)

An evaluation of congenital talipes equinovarus patients treated by various methods [PDF]

open access: yes, 2020
Background: Idiopathic congenital talipes equinovarus is one of the commonest congenital anomaly. Although treatment provides many options, near universal agreement exists that initial management should consist of gentle manipulation of the affected foot.
Sharma, Mohit   +2 more
core   +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

The EUROmediCAT Network and Databases: A Resource for Pharmacovigilance in Pregnancy

open access: yesPharmacoepidemiology and Drug Safety, Volume 35, Issue 5, May 2026.
ABSTRACT Background The evidence gap relating to the risk of congenital anomalies (CA) associated with first trimester medication exposure in pregnancy is well recognized. Aims We describe the EUROmediCAT network and databases, and the methodological approach to pregnancy pharmacovigilance.
Helen Dolk   +27 more
wiley   +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

Assessment of talipes equinovarus treated by Ponseti technique:Three-year preliminary report

open access: yes, 2012
The Ponseti method has become increasingly popular in the treatment of congenital talipes equinovarus (CTEV). Current methods of assessment focus on clinical, functional and radiological outcomes which are subjective and often difficult to repeat ...
Wang, W; id_orcid   +5 more
core   +1 more source

Educational Attainment of Children With Major Congenital Anomalies During Primary School in England: A Population Cohort Study

open access: yesPaediatric and Perinatal Epidemiology, Volume 40, Issue 4, Page 511-525, May 2026.
ABSTRACT Background Major congenital anomalies (CA) affect 2.3% of livebirths and are associated with lower educational attainment. Understanding attainment trajectories throughout primary school would inform parents, schools and organisations and help plan support.
Joachim Tan   +11 more
wiley   +1 more source

Clubfoot: an updated review

open access: yesJournal of the Foot & Ankle
Congenital talipes equinovarus, commonly referred to as clubfoot, is one of the most frequent congenital deformities of the lower limb. Over the last few decades, a major paradigm shift has occurred in its management, with the Ponseti method becoming ...
Alexandre Francisco de Lourenço
doaj   +1 more source

Apert Syndrome Presenting with Omphalocele [PDF]

open access: yesJournal of Krishna Institute of Medical Sciences University, 2019
Apert syndrome is a congenital acrocephalosyndactyly syndrome. It is mainly presented by craniosynostosis, syndactyly of the hands and feet and dysmorphic facial features.
Keerti Swarnkar   +4 more
doaj  

Radiographic Assessment of Congenital Talipes Equinovarus: Strapping versus Forced Dorsiflexion

open access: yesJournal of Orthopaedic Surgery, 2005
Purpose. To compare 2 radiographic assessment methods for congenital talipes equinovarus: strapping the ankle with tapes versus dorsiflexion with a wooden block. Methods. Anteroposterior and lateral radiographs were taken with the ankle strapped by tapes
EHK Yeung, YH Li, ON Ng, W Chow
doaj   +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

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