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137 Possible Causes for Delayed Acquisition of Motor Skills, Mild Rib Sclerosis

  • Achondroplasia

    Spine radiograph lateral view (b) demonstrating mild platyspondyly and expansion of anterolateral parts of the ribs with “club-shaped” configuration (arrows).[] The changes involve areas of bone sclerosis intermingled with areas of resorption.[]

  • Infantile-Onset Ascending Hereditary Spastic Paralysis

    Infantile-onset ascending hereditary spastic paralysis (IAHSP) is a rare, early-onset autosomal recessive motor neuron disease associated with mutations in ALS2. We studied a 17-year-old boy who had features of IAHSP. We also reviewed the current literature on ALS2-related syndromes. Clinical and neuroimaging[…][]

    Missing: Mild Rib Sclerosis
  • Dejerine-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[] […] 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[] Occasionally there could be vision problems, hearing loss and delay in acquisition of motor skills in children. Treatment for this condition is symptomatic.[]

    Missing: Mild Rib Sclerosis
  • Mowat-Wilson Syndrome

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

    Missing: Mild Rib Sclerosis
  • 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[] […] of gross motor skills.[] Barth syndrome is also associated with abnormally diminished muscle tone (hypotonia ), and muscle weakness (skeletal myopathy), that often leads to delays in the acquisition[]

    Missing: Mild Rib Sclerosis
  • Classic Multiminicore Myopathy

    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.[] Poor or decreased motor abilities, delay or arrest of motor milestones, and joint or spinal deformities are often the presenting features of CMD.[]

    Missing: Mild Rib Sclerosis
  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2N

    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[…][]

    Missing: Mild Rib Sclerosis
  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2M

    Disease Type of connection Congenital muscular dystrophy without intellectual disability Familial isolated dilated cardiomyopathy Muscle-eye-brain disease Walker-Warburg syndrome Proximal myotonic myopathy Synonym(s): - LGMD2M Classification (Orphanet): - Inborn errors of metabolism - Rare cardiac disease - Rare[…][]

    Missing: Mild Rib Sclerosis
  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2K

    Vikram Patel, Alistair Woodward, Valery Feigin, Stella R. Quah, Kristian Heggenhougen Academic Press, ٠٧‏/٠٦‏/٢٠١٠ - 560 من الصفحات Colin Mathers who leads the Global Burden of Disease group in WHO has confirmed that, in the 2004 GBD, 13.1% of global Daily Adjusted Life Years are attributable to mental or neurological[…][]

    Missing: Mild Rib Sclerosis
  • Autosomal Recessive 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[…][]

    Missing: Mild Rib Sclerosis

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