Create issue ticket

753 Possible Causes for Joint Stiffness, Pediatric Disorder, Progressive Contractures

  • Arthrogryposis Multiplex Congenita

    Abstract Arthrogryposis multiplex congenita (AMC) is a rare disorder characterized by non-progressive, multiple contractures.[ncbi.nlm.nih.gov] Most recently, through her personal contracting agency she has been supplying consultative PT services to adults with pediatric disorders. Dr.[amcsupport.org] Arthrogryposis multiplex congenita (AMC) is a complex disorder that leads to joint stiffness and deformities in 2 or more joints in afflicted children.[ncbi.nlm.nih.gov]

  • Mucopolysaccharidosis 2

    Flexion contractures. Progressive deafness - usually mixed sensorineural/conductive variety.[patient.info] Abstract Mucopolysaccharidosis type II (MPSII) is an inherited disorder due to a deficiency of the lysosomal enzyme iduronate-2-sulfatase (IDS).[ncbi.nlm.nih.gov] Bone and joint involvement leads to skeletal deformities and joint stiffness.[symptoma.com]

  • Hemophilia

    This disease can lead to further symptoms such as: • progressive decreased motion • flexion contractures • muscle atrophy [1] The second most common presentation of hemophilia[physio-pedia.com] John Akabutu Comprehensice Centre for Bleeding DisordersPediatric Division Stollery Children’s Hospital Clinic Director Dr.[hemophilia.ca] Ultimately this process will cause chronic joint stiffness and pain.[emedicinehealth.com]

  • Mucopolysaccharidosis

    ; hip containment surgeries; corrective osteotomy for progressive valgus deformity at the knee; posterior spinal fusion Multispecialty care is mandatory for these patients[emedicine.medscape.com] The mucopolysaccharidoses: a heterogeneous group of disorders with variable pediatric presentations. J Pediatr. 2004 May;144(5 Suppl):S27-34. Review.[ghr.nlm.nih.gov] Adv Pediatr 33:269–302, 1986. PubMed Google Scholar 17. Muenzer J: The mucopolysaccharidoses: a heterogeneous group of disorders with variable pediatric presentations.[link.springer.com]

  • Mucolipidosis

    Growth generally doesn’t progress beyond the 10th percentile and is complicated by progressive contractures.[invitae.com] Abstract Mucolipidosis II (ML-II) is a pediatric disorder caused by defects in the biosynthesis of mannose 6-phosphate, the carbohydrate recognition signal responsible for[ncbi.nlm.nih.gov] However; the patients with late onset and/or mild joint stiffness experienced slowly progressive symptoms.[ncbi.nlm.nih.gov]

  • Mucopolysaccharidosis 1

    Progressive upper airway disease leads to obstructive sleep apnoea.[patient.info] ., The mucopolysaccharidoses: a heterogeneous group of disorders with variable pediatric presentations. J Pediatr, 2004. 144(5 Suppl): p. S27-34. 2). Beesley, C.E., D.[egl-eurofins.com] The mucopolysaccharidoses: a heterogeneous group of disorders with variable pediatric presentations. J Pediatr. 2004 May;144(5 Suppl):S27-34. Review.[ghr.nlm.nih.gov]

  • Mucopolysaccharidosis 3

    Coarse facies, mild dysostosis multiplex, hepatosplenomegaly and joint contractures may also be present.[genedx.com] Mucopolysaccharidosis III is considered the most common of these genetic disorders, occurring with an incidence of 1 in 70,000 newborns.[emedicine.medscape.com] stiffness, vertebral bodies and hypertrichosis.[phoenixnestbiotech.com]

  • Mucopolysaccharidosis 1H

    The two patients with graft failure (patients 14 and 15) experienced progressive contractures in almost all joints.[ojrd.biomedcentral.com] Pediatrics. 1999;103(6):1158–66. View Article PubMed Google Scholar Manikam R, Perman JA. Pediatric feeding disorders. J Clin Gastroenterol. 2000;30(1):34–46.[ojrd.biomedcentral.com] Joint stiffness: Joint stiffness occurs by the age of 2 years and is progressive. There is a characteristic claw-hand deformity due to phalangial dysostosis.[symptoma.com]

  • Winchester Syndrome

    The syndrome is characterized by dissolution of carpal and tarsal bones with generalized osteoporosis, progressive joint contractures, short stature, peripheral corneal opacities[ncbi.nlm.nih.gov] Definition / general Rare hereditary pediatric disorder with extracellular hyaline material deposition in skin, soft tissue and bone Terminology Molluscum fibrosum in children[pathologyoutlines.com] The syndrome is characterized by short stature, coarse face, corneal opacities, generalized osteolysis and progressive painful arthropathy with joint stiffness and contractures[ncbi.nlm.nih.gov]

  • Progeria

    During the first to third year the following usually become apparent: partial alopecia progressing to total alopecia, loss of subcutaneous fat, progressive joint contractures[flybase.org] Haller, Caffey's Pediatric Diagnostic Imaging 10th ed. Mosby, 2004: 2212- 2213.[ijri.org] Children typically experience medical issues that are usually associated with older age, such as hair loss, bone changes, hearing loss, joint stiffness, atherosclerosis (hardening[thinkgenetic.com]

Similar symptoms