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524 Possible Causes for Pediatric Disorder, Waddling Gait

  • Familial Hypophosphatemia

    gait, muscle pain and weakness.[ultragenyx.com] 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] X-linked dominant inheritance works differently depending upon whether the mother (left image) or father (right image) is the carrier of a gene that causes a disease or disorder[en.wikipedia.org]

  • Duchenne Muscular Dystrophy

    At age 4 he had a waddling gait and could no longer climb stairs.[ncbi.nlm.nih.gov] Duchenne muscular dystrophy (DMD) is a lethal progressive pediatric muscle disorder and genetically inherited as an X-linked disease that caused by mutations in the dystrophin[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

    gait, and laxity of joints.[ncbi.nlm.nih.gov] 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]

  • Schmid Metaphyseal Chondrodysplasia

    gait.[ncbi.nlm.nih.gov] External links Metaphyseal chondrodysplasia, Jansen type — OrphaNet Information (PDF) Jansen’s Metaphyseal Chondrodysplasia, Case Report, Indian Pediatrics Jansen Type Metaphyseal[checkrare.com] […] metaphyseal chondrodysplasia (SMCD; MIM 156500) is an autosomal dominant disorder of the skeleton that is manifested in early childhood by short stature, coxa vara, and a waddling[ncbi.nlm.nih.gov]

  • 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] 1 Department of Pediatric Endocrinology and Diabetes, Konya Training and Research Hospital, Meram/Konya, Turkey; 2 Department of Pediatric Endocrinology and Diabetes, School[bone-abstracts.org] gait Premature tooth loss, particularly of the incisors The disease may spontaneously resolve, but may also return in adulthood.[everydayhealth.com]

  • Coxa Vara

    Congenital Coxa Vara (coxa vara) Deformity Congenital coxa vara Most patient with coxa varus deformity complains about limping or waddling gait, besides hip pain.[istanbulorthopedics.com] 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[en.wikipedia.org]

  • Slipped Capital Femoral Epiphysis

    Signs may include waddling gait, decreased range of motion and a painful limp. The range of motion is also restricted.[luriechildrens.org] MR Imaging of Congenital/Developmental and Acquired Disorders of the Pediatric Hip and Pelvis.[radsource.us] gait externally rotated leg on the affected side inability to bear weight limited range of motion of the hip Imaging Radiography indication for all patients to confirm diagnosis[medbullets.com]

  • Mucolipidosis

    However, in four patients presented here, initial finding was knee pain or waddling gait, which started between six-16years of age.[ncbi.nlm.nih.gov] Mucolipidosis II (ML-II) is a pediatric disorder caused by defects in the biosynthesis of mannose 6-phosphate, the carbohydrate recognition signal responsible for targeting[ncbi.nlm.nih.gov] The severe pediatric disorder mucolipidosis II (ML-II; also known as I-cell disease) is caused by defects in mannose 6-phosphate (Man-6-P) biosynthesis.[ncbi.nlm.nih.gov]

  • Becker Muscular Dystrophy

    From age 27 years, he developed proximal muscle weakness predominantly of the lower limbs, a positive Gower sign, and a waddling gait.[ncbi.nlm.nih.gov] Little is known about parental motivations and expectations for clinical trials for rare pediatric disorders.[ncbi.nlm.nih.gov] Other symptoms may include: Muscle weakness that starts in the pelvis, shoulders, hips, and thighs Waddling gait Walking on the toes Larger-than-normal calves Muscle cramps[webmd.com]

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