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660 Possible Causes for Abnormal Gait, Coarse Facial Features

  • Mucopolysaccharidosis

    Hypermobile joints and an abnormal gait with a tendency to fall may also be presenting features.[genedx.com] facial features, developmental delay, and an elevated quantitative urine glycosaminoglycan (GAG) level.[ncbi.nlm.nih.gov] Twelve patients had a waddling gait. Four patients were partially wheelchair-dependent and ten patients had limitations in their maximum walking distance.[ncbi.nlm.nih.gov]

  • Mucopolysaccharidosis 1

    Hypermobile joints and an abnormal gait with a tendency to fall may also be presenting features.[genedx.com] Further common findings are coarse facial features, carpal tunnel syndrome, umbilical and inguinal hernia, and hepatomegaly.[symptoma.com] Dental abnormalities Pectus carinatum, kyphosis, scoliosis, genu valgum, hypermobile joints Waddling gait with frequent falls Qualitative urine glycosaminoglycan (GAG) analysis[centogene.com]

  • Winchester Syndrome

    Elevated IL1-beta Elevated IL6 Elevated antinuclear antibody (ANA) (speckled pattern) Performance Abnormal gait Skeletal Carpal osteolysis Fusiform finger swelling Interphalangeal[datagenno.com] Affiliated tissues include bone , skin and testes , and related phenotypes are gingival overgrowth and coarse facial features OMIM : 57 Winchester syndrome presents with severe[malacards.org] At the age of 18 months, her parents observed an abnormal gait and an element of contractures appeared.[ped-rheum.biomedcentral.com]

  • Mucopolysaccharidosis 6

    Affected individuals may develop pain, especially of the joints and hip, spinal cord compression, an abnormal manner of walking (gait), or difficulty walking.[rarediseases.org] Physical Facial features associated with MPS VI include the following: Coarse facial features (Compare the facial features with those of other family members to best appreciate[emedicine.medscape.com] [symptoma.com] Difficulty Walking Affected individuals may develop pain, especially of the joints and hip, spinal cord compression, an abnormal manner of walking (gait), or[symptoma.com]

  • Mucopolysaccharidosis 3

    One or both hip joints may be underdeveloped, leading to pain and difficulties walking. X-rays reveal a condition similar to Perthes disease, an orthopaedic condition.[socialstyrelsen.se] Other symptoms include: Behavioral problems Coarse facial features Diarrhea Full lips Heavy eyebrows that meet in the middle of the face above the nose Sleep difficulties[mpssociety.org] Dental abnormalities Pectus carinatum, kyphosis, scoliosis, genu valgum, hypermobile joints Waddling gait with frequent falls Qualitative urine glycosaminoglycan (GAG) analysis[centogene.com]

  • Mucopolysaccharidosis 4A

    gait.[cjhr.org] facial features Coarse facial appearance 0000280 Constricted iliac wings 0003277 Coxa valga 0002673 Disproportionate short-trunk short stature Disproportionate short-trunked[rarediseases.info.nih.gov] Signs & Symptoms Individuals with MPS disorders share many similar symptoms such as multiple organ involvement, distinctive “coarsefacial features, and abnormalities of[rarediseases.org]

  • Chronic Alcoholism

    Brain damage Alcohol is associated with blurred vision, memory lapses, slurred speech, difficulty walking and slowed reaction time.[medicalnewstoday.com] Wernicke's syndrome results in disordered eye movements, very poor balance, and difficulty walking.[medical-dictionary.thefreedictionary.com] Examination of the nervous/muscular system may show damage to many nerve systems: Abnormal eye movement Decreased or abnormal reflexes Fast pulse (heart rate) Low blood pressure[medlineplus.gov]

  • Mucopolysaccharidosis 4

    Hypermobile joints and an abnormal gait with a tendency to fall may also be presenting features.[genedx.com] Children with spine and bone conditions can have difficulty walking and may require a wheelchair; others may be more mobile.[chop.edu] At age 3 years, the patient had kyphosis, and an abnormal gait was present by age 5 years.[emedicine.medscape.com]

  • Coxa Valga

    It tends to go unnoticed until walking age is reached, when the deformity results in a leg length difference or abnormal gait pattern.[physio-pedia.com] (AFA) and hypertrichosis and acromegaloid facial features (HAFF) are characterized by congenital hypertrichosis; distinctive coarse facial features (including broad nasal[ncbi.nlm.nih.gov] Diagnosis can be complicated since the source of the problem – causing pain or difficulty walking, sitting, or standing – may not be immediately apparent.[hss.edu]

  • Mucopolysaccharidosis 1H

    Common symptoms of MPS 1 may include: abdominal hernia, abnormal gait, coarse features , developmental delay, gibbus deformity, hand/wrist pain, hepatosplenomegaly, joint[raredr.com] Note his coarse facial features, crouched stance, thickened digits, and protuberant abdomen. Transgenic mice with a targeted disruption of a -L-iduronidase .[medgen.genetics.utah.edu] […] hairy skin all over the body, a tuft of hair in the parietal region, coarse facial features and a prominent forehead with a large tongue, hepatosplenomegaly and skeletal[dx.doi.org]

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