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245 Possible Causes for Delayed Acquisition of Motor Skills, Focal Dystonia - Upper Limb

  • Infantile-Onset Ascending Hereditary Spastic Paralysis

    […] epilepsy syndrome Costello syndrome Crane-Heise syndrome Cranial nerve and nuclear aplasia Cranio-cervical dystonia with laryngeal and upper-limb involvement Craniodigital-intellectual[se-atlas.de] limb-onset distal myopathy Floating-Harbor syndrome Flynn-Aird syndrome Focal dermal hypoplasia Focal epilepsy-intellectual disability-cerebro-cerebellar malformation Focal[se-atlas.de] […] with intellectual disability Ferro-cerebro-cutaneous syndrome Fetal akinesia-cerebral and retinal hemorrhage syndrome Filippi syndrome Fingerprint body myopathy Finnish upper[se-atlas.de]

  • Infantile-Onset Autosomal Recessive Nonprogressive Cerebellar Ataxia

    […] epilepsy syndrome Costello syndrome Crane-Heise syndrome Cranial nerve and nuclear aplasia Cranio-cervical dystonia with laryngeal and upper-limb involvement Craniodigital-intellectual[se-atlas.de] limb-onset distal myopathy Floating-Harbor syndrome Flynn-Aird syndrome Focal dermal hypoplasia Focal epilepsy-intellectual disability-cerebro-cerebellar malformation Focal[se-atlas.de] […] with intellectual disability Ferro-cerebro-cutaneous syndrome Fetal akinesia-cerebral and retinal hemorrhage syndrome Filippi syndrome Fingerprint body myopathy Finnish upper[se-atlas.de]

  • Déjerine-Sottas Disease

    acquisition of motor skills Mild loss of hearing Limitation in eye movements Reduced muscle tone This condition can be diagnosed from the symptoms as well as your child’s[kidbones.net] […] in acquisition of motor skills in childhood occasionally, limitation of eye movements or other eye problems occasionally, mild hearing loss How does Dejerine-Sottas Disease[mda.org.au] Occasionally there could be vision problems, hearing loss and delay in acquisition of motor skills in children. Treatment for this condition is symptomatic.[turmericforhealth.com]

    Missing: Focal Dystonia - Upper Limb
  • Mowat-Wilson Syndrome

    The mental retardation, usually severe, was constant; the delay in the acquisition of motor skills was more variable (table 2).[doi.org]

    Missing: Focal Dystonia - Upper Limb
  • Barth Syndrome

    acquisition of gross motor skills Exercise intolerance Muscle weakness Easily fatigued Chronic or recurrent diarrhea Feeding problems in infancy, "picky eating" in children[verywellhealth.com] […] of gross motor skills.[rarediseases.org] Barth syndrome is also associated with abnormally diminished muscle tone (hypotonia ), and muscle weakness (skeletal myopathy), that often leads to delays in the acquisition[medium.com]

    Missing: Focal Dystonia - Upper Limb
  • Rigid Spine Syndrome

    Since delay of motor skill acquisition may be a presenting symptom of CMD, onset of manifestations before age two years may be a reasonable diagnostic criterion.[ncbi.nlm.nih.gov] Poor or decreased motor abilities, delay or arrest of motor milestones, and joint or spinal deformities are often the presenting features of CMD.[ncbi.nlm.nih.gov]

    Missing: Focal Dystonia - Upper Limb
  • Muscular Dystrophy-Dystroglycanopathy Type C2

    Primary Outcome Measures : MRI scan for qualitative analysis of muscle involvement [ Time Frame: One MRI scan per subject (exam lasts approximately 60 min.) ] The MRI protocol include T1-weighted brain and whole body examination. Four cross-sectional slices at shoulder, lumbar back, thigh and calf are chosen for[…][clinicaltrials.gov]

    Missing: Focal Dystonia - Upper Limb
  • Muscular Dystrophy-Dystroglycanopathy Type C4

    E. Gilbert-Barness, L.A. Barness, P.M. Farrell IOS Press, 06.01.2017 - 960 Seiten The 2nd Edition of Metabolic Diseases provides readers with a completely updated description of the Foundations of Clinical Management, Genetics, and Pathology. A distinguished group of 31 expert authors has contributed 25 chapters as a[…][books.google.de]

    Missing: Focal Dystonia - Upper Limb
  • Muscular Dystrophy-Dystroglycanopathy Type C1

    Chapter First Online: 27 June 2014 Abstract LGMD2K is caused by mutations in the POMT1 gene, encoding for O-mannosyl-transferase-1 protein (Table 16.1), and results from defective glycosylation of alpha-dystroglycan. This disorder represents the mildest end of the phenotypic spectrum of muscular dystrophies[…][link.springer.com]

    Missing: Focal Dystonia - Upper Limb
  • Limb-Girdle Muscular Dystrophy Type 2Q

    Autosomal recessive limb-girdle muscular dystrophy-17 is characterized by early childhood onset of proximal muscle weakness and atrophy without skin involvement. One family has shown rapid progression of the disorder in adolescence (summary by Gundesli et al., 2010). For a discussion of genetic heterogeneity of[…][ncbi.nlm.nih.gov]

    Missing: Focal Dystonia - Upper Limb

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