Results 61 to 70 of about 4,548 (220)

A constellation of orthopaedic deformities in connection with cartilage oligomeric matrix protein mutation

African Journal of Paediatric Surgery, 2019
Background: Trendelenburg's gait can be observed in Legg-Calvé-Perthes disease, antalgic gait observed in osteoarthropathy and waddling gait is usually seen in genu varum and circumduction gait in patients with genu valgum.
Ali Al Kaissi, Maher Ben Ghachem, Vladimir Kenis, Eugene Melchenko, Franz Grill, Rudolf Ganger, Susanne Gerit Kircher   +6 more
doaj   +1 more source

Prevalence of lower limb deformities among primary school students

Egyptian Rheumatology and Rehabilitation, 2021
Background Lower limb deformities could affect child's quality of life and may worsen with time. This work aims to study the prevalence of lower limb deformities among primary school students in our governorate.
Sahar Saad Ganeb, Sami El-Said Egaila, Abdelmoniem Abdelfattah Younis, Asmaa Moheiy Abd El-Aziz, Nashwa Ismail Hashaad   +4 more
doaj   +1 more source

X‐Linked Hypophosphatemia Caused by a New Partial Insertion of LINE‐1 in the PHEX Gene

Human Mutation, Volume 2026, Issue 1, 2026.
X‐linked hypophosphatemia (XLH), primarily caused by mutations of the PHEX gene, is the most common cause of genetic rickets. Pediatric cases of XLH typically present with elevated levels of serum fibroblast growth factor 23 (FGF23), hypophosphatemia, rickets, and impaired growth.
Dongmei Li, Wan Peng, Lu Kang, Jia Geng, Yu Lu, Jing Lu, Chen Jian-Min   +6 more
wiley   +1 more source

O Estudo da osteotomia valgizante proximal de tíbia com placa "calço" de puddu. [PDF]

, 2001
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Clínica Cirúrgica, Curso de Medicina, Florianópolis ...
Carvalho, Daniel de Souza
core  

Further Evidence That Chondrocalcinosis 1 (CCAL1) is a Confirmed Mendelian Phenotype With a Known Molecular Basis

American Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.
ABSTRACT Chondrocalcinosis (CCAL), also known as calcium pyrophosphate dihydrate deposition disease (CPPDD), is a frequent multifactorial condition in the elderly, but there are two rare autosomal dominant Mendelian forms, CCAL1 (OMIM %600668) and CCAL2. Only three families with molecularly proven CCAL1 have been reported.
Anna‐Christina Pansa, Mareike Selig, Markus Wingendorf, Matthew A. Brown, Oliver Bartsch   +4 more
wiley   +1 more source

Evaluation of the Knee Anatomical Deformities and Its Relationship with Hip Joint [PDF]

Journal of Mazandaran University of Medical Sciences
Background and purpose: Knee joint disorders are divided into two general categories of traumatic and non-traumatic injuries, including skeletal deformities such as genu valgum (knocked knee) and genu varum (bowed legs).
Abbas Heidari-Moghadam, Yousef Asadi-Fard, Zeinab Najaf-Abadi, Hodasadat Sharif, Afrooz Moradkhani   +4 more
doaj  

Proksimal tibial osteotomi cerrahisinde turnike kullanımı sonrası gelişen rabdomiyoliz: Olgu sunumu ve literatu¨r taraması

Acta Orthopaedica et Traumatologica Turcica, 2020
Havalı turnike kullanımı sonrası rabdomiyoliz gelişimi oldukça nadir göru¨len bir komplikasyondur. Bu çalışmada; proksimal tibia osteotomi cerrahisi sonrasında karşılaşılan olağan dışı bir turnike komplikasyonunu sunmayı amaçladık.
Ismail TURKMEN, Irfan ESENKAYA, Koray UNAY, Mehmet Akif AKÇAL   +3 more
doaj   +1 more source

Anthropometric analysis of the evolution of the physiological Genu Varus and Valgus in childhood by measuring the medial femoral intercondylar and the medial intermalleolar distances [PDF]

, 2014
Los cambios morfológicos del eje de miembros inferiores se expresan por un genu varo y valgo fisiológico en la niñez. La evolución de los ángulos, torsiones y rotaciones del esqueleto son determinantes en este proceso.
Cabral, Maria Eugenia, Facciuto, Franco, Feldman, Sara, Gargano, Santiago Guillermo   +3 more
core  

Beyond Nutritional Deficiency: Persistent Rickets as a Manifestation of Vitamin D‐Dependent Rickets Type II in a Toddler

Clinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Vitamin D‐dependent rickets type II (VDDR‐II) is a rare hereditary disorder caused by mutations in the vitamin D receptor gene, resulting in resistance to active vitamin D and impaired calcium absorption. We report a 2‐year and 6‐month‐old female toddler presenting with persistent rickets, delayed motor milestones, dental abnormalities, and ...
Abhisek Jha, Anil Yadav, Uma Shankar Jha, Preethuja Shah, Rohan Kumar Shah, Kuldeep Timilsina, Prabha Jha, Aabish Dahal, Saugat Bagale   +8 more
wiley   +1 more source

The Assessment of Bone Metabolısm Parameters in Paedıatrıc patıents wıth Genu varum and Genu valgus deformıtıes

Acta Medica Alanya
Aim: There are a limited number of studies in the literature explaining the relationship between bone metabolism parameters such as vitamin D, calcium (Ca), parathormone (PTH), magnesium (Mg), and alkaline phosphatase (ALP) and pediatric lower extremity ...
Sefa Key, Şükrü Demir, Hüseyin Kürüm   +2 more
doaj   +1 more source