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344 Possible Causes for Pediatric Disorder, Waddling Gait

  • Schmid Metaphyseal Chondrodysplasia

    External links Metaphyseal chondrodysplasia, Jansen type — OrphaNet Information (PDF) Jansen’s Metaphyseal Chondrodysplasia, Case Report, Indian Pediatrics Jansen Type Metaphyseal[checkrare.com] gait.[ncbi.nlm.nih.gov] Jansen Type Metaphyseal Chondrodysplasia -- National Organization for Rare Disorders (NORD) A Novel Parathyroid Hormone (PTH)/PTH-Related Peptide Receptor Mutation in Jansen[en.wikipedia.org]

  • Congenital Hip Dysplasia

    gait.[healthpoint.co.nz] Four all-new chapters: Pediatric Physical Therapy, Cultural Sensitivity and Family-Centered Care; Traumatic Injury to the Central Nervous System: Spinal Cord Injury; Traumatic[books.google.de] Depending on their severity at the time initial presentation, a pediatric specialist may provide surgical treatment.[drmclawhorn.com]

  • Hypophosphatasia

    gait.[ncbi.nlm.nih.gov] - PEDIATRIC Patients » Helpful information about Applying for Disability Benefits with an Endocrine Related Disorder - ADULT patients » Click here for member benefits or[magicfoundation.org] gait Premature tooth loss, particularly of the incisors The disease may spontaneously resolve, but may also return in adulthood.[everydayhealth.com]

  • Duchenne Muscular Dystrophy

    At age 4 he had a waddling gait and could no longer climb stairs.[ncbi.nlm.nih.gov] BACKGROUND AND PURPOSE: Duchenne muscular dystrophy (DMD) is a lethal progressive pediatric muscle disorder and genetically inherited as an X-linked disease that caused by[ncbi.nlm.nih.gov] Additional early signs and symptoms include: Developmental delay Muscle weakness Clumsiness Waddling gait Difficulty or inability to perform activities such as climbing stairs[pfizer.com]

  • Mucopolysaccharidosis

    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] gait, and laxity of joints.[ncbi.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]

  • Familial Hypophosphatemia

    Genetic disorders of phosphate regulation. Pediatr Nephrol. 2012;27(9):1477-87. Carpenter TO, Imel EA, Holm IA, Jan de Beur SM, Insogna KL.[rarediseases.org] gait, muscle pain and weakness.[ultragenyx.com] There are at least two factors that have brought genetic disorders into the forefront of pediatrics.[books.google.com]

  • Camurati-Engelmann Syndrome

    Pediatrics 1984 ; 74 : 399 –405. 3 Crisp AJ, Brenton DP. Engelmann's disease of bone—a systemic disorder?[academic.oup.com] A waddling gait (48%), easy fatigability (44%), and muscle weakness (39%) were other important features.[ncbi.nlm.nih.gov] Brenton Engelmann's disease of bone-a systemic disorder? Ann Rheum Dis, 41 (1982), pp. 183-188 4 K. Janssens,F. Vanhoenacker,M. Bonduelle,L.[reumatologiaclinica.org]

  • Coxa Vara

    […] with hyperlordosis of spine & waddling gait - limb-length discrepancy - trendelenburg sign - mimic DDH Gait - short-leg - trendelenburg sag - abductor lurch - if bilateral[52.62.202.235] Abstract Developmental coxa vara (DCV) is a well-known pediatric hip disorder that is associated with triplanar deformity of the proximal femur.[ncbi.nlm.nih.gov] D Resnick: Diagnosis of Bone and Joint Disorders Vol V, Saunders 1995, ISBN 0-7216-5071-6 External links [ edit ][en.wikipedia.org]

  • Dyggve-Melchior-Clausen Syndrome

    gait, and radiographic findings of irregular iliac crests and flattening of vertebral bodies; autosomal recessive inheritance.[medical-dictionary.thefreedictionary.com] Author information 1 Pediatric Orthopedic Institute n.a. H.[ncbi.nlm.nih.gov] Center for Human Genetics and is Director of the Rare Brain Disorders Program (Clinic and Laboratory).[books.google.com]

  • Erb Muscular Dystrophy

    Contractures Tachypnea and shortness of breath Assessment-Duchenne and Becker's types Wide stance and waddling gait Gowers' sign when rising from a sitting or supine position[quizlet.com] Neuromuscul Disord . 2009 Mar. 19(3):182-8. [Medline] . Rosales XQ, Tsao CY. Childhood onset of limb-girdle muscular dystrophy. Pediatr Neurol . 2012 Jan. 46(1):13-23.[emedicine.medscape.com] Weakness of the hip and upper leg muscles may cause a distinctive waddling gait.[rarediseases.org]

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