Results 11 to 20 of about 16,290 (203)

Cri du Chat Syndrome and congenital dislocation of the hips and knees [PDF]

open access: yesRevista de la Facultad de Ciencias Médicas de Córdoba
Introduction: Cri Du Chat Syndrome (CdCS) is an autosomal genetic disorder involving the complete or partial deletion of the short arm of chromosome 5 (5p). The size of the CdCS deletion ranges from approximately 10-45 Mb.
Natã Nascimento de Jesus Graça   +2 more
doaj   +2 more sources

Congenital Dislocation of the Hip [PDF]

open access: yesBMJ, 1960
Treatment of congenital dislocation of the hip depends on the age of the patient and on the assessment of the particular pathological factors present at the different stages of displacement. Treatment at birth by routine examination for the ‘clunk’ sign is the only reliable method whereby normal joint development can be anticipated in almost every ...
E. W. Somerville, J. C. Scott
  +17 more sources

Analysis of the epidemiological profile of congenital hip deformities, 2011–2021 [PDF]

open access: yesRevista Paulista de Pediatria, 2023
Objective: This study aimed to identify the relevance of hospitalizations for congenital hip deformities in Bahia. Methods: This is a retrospective epidemiological study in public databases.
Bianca Gabriella de Oliveira   +3 more
doaj   +1 more source

THE EPIDEMIOLOGY OF DEVELOPMENTAL DYSPLASIA OF THE HIP IN MALES [PDF]

open access: yesActa Ortopédica Brasileira, 2020
Developmental Dysplasia of the Hip (DDH) is one of the most common orthopedic hip diseases of the pediatric population. There is a predominance in females and patients with known risk factors.
Ellen de Oliveira Goiano   +3 more
doaj   +1 more source

Early detection and risk factors of congenital hip dislocation in Morocco

open access: yesJournal of Public Health in Africa, 2023
Background and Objective: Congenital dislocation of the hip is a malformation of the lower limbs that could be complicated by a disabling physical handicap with long-term psychological and social repercussions if detected late.
Adri Ilham   +2 more
doaj   +1 more source

Treatment of congenital hip dislocation before the walking age

open access: yesLa Pediatria Medica e Chirurgica, 2022
The worst type of hip developmental dysplasia, known as congenital hip dislocation (CHD), is characterized by acetabular cavity, proximal femoral segment, and ligamentus capsule apparatus dysmorphisms that result in partial or total loss of the hip ...
Daniele Sini   +2 more
doaj   +1 more source

ORTHOPEDIC ASSESSMENT OF THE HIPS IN NEWBORNS AFTER INITIAL PEDIATRIC SURVEY [PDF]

open access: yesActa Ortopédica Brasileira, 2019
Objective: To analyze and follow-up patients previously selected by pediatricians at the time of birth who presented altered initial physical examination results to identify the pathological changes in their hips. Methods: A prospective cohort study was
Felipe Chioro Gonzalez   +5 more
doaj   +1 more source

Congenital dislocation of the hip – theories, etiological and predisposing factors (risk factors)

open access: yesСибирский научный медицинский журнал, 2022
According to current statistics worldwide, congenital orthopedic pathologies rank second quantitatively after congenital diseases of the nervous system.
N. Yu. Pakhomova   +4 more
doaj   +1 more source

Open and Closed Reduction for Developmental Dysplasia of the Hip in New York State: Incidence of Hip Reduction and Rates of Subsequent Surgery. [PDF]

open access: yes, 2020
BackgroundThere are limited data on the incidence and outcomes of open and closed hip reduction in patients with developmental dysplasia of the hip (DDH).
Chang   +14 more
core   +1 more source

Orthosis Treatment for Patients with Congenital Hip Dislocation

open access: yesSurabaya Physical Medicine and Rehabilitation Journal, 2023
Background: Congenital dislocation of the hip is currently a public health and socioeconomic problem. Delayed treatment impairs the functional prognosis of the affected hip and increases the need for surgical treatment.
Manohisoa Nomena Harisambatra Rakotonandrianina   +3 more
doaj   +1 more source

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