Results 21 to 30 of about 587,940 (173)
CONGENITAL DISLOCATION OF THE HIP IN IDENTICAL TWINS
, 1959 1. Congenital dislocation of the hip in identical twins is reported. 2. The heredity of congenital dislocation of hip is discussed. Studies in twins show that congenital dislocation of hip is probably a hereditary dysplasia of the acetabulum and upper ...
P. Buri, M. Geiser
core +1 more source
Гений oртопедии, 2020 Congenital hip dislocation in adults (Crowe type IV) is an indication for hip replacement. Shortening subtrochanteric osteotomy of the femur reduces the risk of vascular and neurological complications and corrects the antetorsion of the proximal femur ...
Lev S. Shnaider +5 more
doaj +1 more source
Screening for Congenital Hip Dislocation—An Overview
, 2023 Developmental dysplasia of the hip, previously known as congenital dislocation of the hip, is the most common congenital disease of the musculoskeletal system in newborns.
Vlad Dima +2 more
core +1 more source
Congenital Hip Dislocation: A Rare Case in Adulthood
Acta Médica Portuguesa, 2018 - / -
Natália Ferreira +2 more
doaj +1 more source
Advanced Science, EarlyView.This article aims to elucidate the biological mechanisms of bone repair and the evolution of material design, highlighting key cellular and molecular processes. It further proposes strategies and prospects for programmable bio‐interactive materials, which enable precisely guided bone tissue regeneration by dynamically regulating cell behavior and the ...
Qingrui Fan +6 more
wiley +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT ADNP‐related Helsmoortel–Van der Aa syndrome (ADNP‐related HVDAS) is a single gene form of autism spectrum disorder (ASD) caused by pathogenic sequence variants in the activity‐dependent neuroprotective protein (ADNP) gene. In addition to ASD, ADNP‐related HVDAS is associated with a wide range of cognitive, behavioral, and physical health ...
Jarrett Fastman +11 more
wiley +1 more source
Severe Headbanging Responsive to Levodopa in a Child With FOXP1 Syndrome
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT We report a 9‐year‐old female with FOXP1 syndrome due to a de novo in‐frame deletion in the FOXP1 gene. The child has a severe neurodevelopmental disorder including global developmental delay and autism spectrum disorder. At age 2, she developed severe headbanging, which was progressive and did not respond to multidisciplinary, behavioral ...
Pamela Veale +2 more
wiley +1 more source
Spontaneous correetlon In the congenital dlslocatlon of the hip
Acta Orthopaedica et Traumatologica Turcica, 2020 1 It was pointed out that the case of congenital hip dysplasia would be spontaneous correction in spite of treatment in the congenital dislocation of the hip has to be obtained by conservative and surgical procedures.\n2 Our case was reported to be ...
Selcuk Atilla
doaj
Гений oртопедии, 2021 Introduction The possibility of gradual closed reduction of hip dislocation in children over 1.5 years old is considered doubtful. Purpose Analysis of long-term results of applying the Ilizarov technique of gradual closed reduction in combination with ...
Mikhail P. Teplenky +2 more
doaj +1 more source
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.ABSTRACT Arthrogryposis Multiplex Congenita (AMC) encompasses several hundred conditions with diverse genetic, pathophysiological, and clinical origins. The overarching EXPLAIN study explores underlying causes and implications of AMC and represents the largest clinical cohort of adults with AMC reported to date.
My Vuong Hermansen +5 more
wiley +1 more source