Create issue ticket

648 Possible Causes for Congenital Hip Dysplasia

  • Osgood-Schlatter Disease

    Osgood–Schlatter disease (OSD) is inflammation of the patellar ligament at the tibial tuberosity. It is characterized by a painful bump just below the knee that is worse with activity and better with rest. Episodes of pain typically last a few weeks to months. One or both knees may be affected and flares may[…][]

  • Mucopolysaccharidosis

    RATIONALE: Mucopolysaccharidosis type VI (MPS VI) or Maroteaux-Lamy syndrome is produced by the deficiency of the enzyme arylsulfatase B, responsible for the hydrolysis of N-acetyl-D-galactosamine, chondroitin sulfate, and dermatan sulfate. PATIENT CONCERNS: A 3-year-old male with Moroccan origins is the index[…][]

  • Turner Syndrome

    ., horseshoe kidney, duplicated or cleft renal pelvis), autoimmune thyroiditis, celiac disease, congenital hip dysplasia, and scoliosis. 11 Girls with Turner syndrome typically[] […] developmental dysplasia of the hip occurs more frequently in girls with Turner syndrome than in the general population. 52, 57 This contributes to the development of arthritis[] […] developmental dysplasia of the hip occurs more frequently in girls with Turner syndrome than in the general population. 52 , 57 This contributes to the development of arthritis[]

  • Congenital Hip Dysplasia

    Congenital hip dysplasia describes a medical condition characterized by an abnormal development of the hip joint. Congenital hip dysplasia is frequently asymptomatic.[] The most reliable sign for the diagnosis of congenital hip dysplasia at birth is the "click" sign.[] Abstract The authors take into consideration the different phases of the treatment of congenital hip dysplasia (CHD) as it is related to age and natural development.[]

  • Mucopolysaccharidosis 2

    Mucopolysaccharidosis II (Hunter syndrome), a lysosomal storage disorder caused by a deficiency of iduronate-2-sulfatase (IDS), has variable clinical phenotypes. Total by nearly 400 different mutations have been identified in IDS gene from patients with Hunter syndrome. Herein, we reported a patient who has a novel[…][]

  • Mucopolysaccharidosis 6

    Maroteaux–Lamy syndrome is a form of mucopolysaccharidosis caused by a deficiency in arylsulfatase B (ARSB). [2] It is named after Pierre Maroteaux (1926–) and his mentor Maurice Emil Joseph Lamy (1895–1975), both French physicians. [3] [4] Symptoms [ edit ] Children with Maroteaux–Lamy syndrome usually have[…][]

  • Ehlers Danlos Syndrome

    Developmental dysplasia of the hip (formerly congenital hip dislocation) occurs in 1% (the arthrochalasis type is characterized by bilateral developmental dysplasia of the[]

  • Seckel Syndrome

    Primary microcephaly represents an example of clinically and genetically heterogeneous condition. Here we describe a case of primary microcephaly from the Karachay-Cherkess Republic, which was initially diagnosed with Seckel syndrome. Clinical exome sequencing of the proband revealed a novel homozygous single[…][]

  • Hip Dysplasia Type Beukes

    Total hip replacement in congenital dislocation and dysplasia of the hip. The Journal of Bone & Joint Surgery , 61(1), pp.15-23.[] Some common causes of hip pain include bursitis, sciatica. Congenital hip dysplasia at Make research projects and school reports about Congenital hip dysplasia easy.[] […] for Beukes familial hip dysplasia Categories : Congenital and Genetic Diseases ; Musculoskeletal Diseases Source: GARD (NIH) 2 • • • References Source: GARD (NIH):[]

  • Congenital Muscular Torticollis

    Associated Conditions Congenital asymmetric contractures of hip abductors Unilateral Congenital Hip Dysplasia Unilateral Metatarsus Adductus V.[] Radiology Neck XRay Indicated for significantly limited neck ROM Ultrasound Hips Assess for concurrent Congenital Hip Dysplasia Indicated for significant hip abductor tightness[]

Further symptoms