Create issue ticket

45 Possible Causes for Onset of Symptoms in First or Second Decade of Life, Shoulder Girdle Weakness, Walking Delay

  • Congenital Merosin-Positive Muscular Dystrophy

    Decreased lung function due to weak breathing muscles 0002747 Scoliosis Abnormal curving of the spine 0002650 Shoulder girdle muscle weakness Weak shoulder muscles 0003547[rarediseases.info.nih.gov] The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] Delayed ability to roll over Delayed ability to stand with support Delayed ability to sit alone Delayed ability to walk alone (nearly half walk after 4 years) Mild facial[checkorphan.org]

  • Limb-Girdle Muscular Dystrophy Type 1E

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] Commonly, pelvic girdle muscles are involved before and much more severely than shoulder girdle muscles.[clevelandclinicmeded.com] In mild forms of MEB, affected individuals experience delays in attaining developmental milestones, but eventually may be able to walk independently.[rarediseases.org]

  • Muscular Dystrophy-Dystroglycanopathy Type C5

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] […] muscle weakness 0003749 Shoulder girdle muscle weakness Weak shoulder muscles 0003547 Waddling gait 'Waddling' gait Waddling walk [ more ] 0002515 5%-29% of people have these[rarediseases.info.nih.gov] […] dystrophy type 2C (LGMD2C) is a subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a childhood onset of progressive shoulder and pelvic girdle[orpha.net]

  • Limb-Girdle Muscular Dystrophy Type 2L

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] […] muscle weakness 0003749 Shoulder girdle muscle weakness Weak shoulder muscles 0003547 Waddling gait 'Waddling' gait Waddling walk [ more ] 0002515 5%-29% of people have these[rarediseases.info.nih.gov] Rare cases are described with a LGMD phenotype. [29, 30] Hypotonia and delayed motor milestones are present, but walking is achieved.[emedicine.medscape.com]

  • Limb-Girdle Muscular Dystrophy Type 2E

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] shoulder-girdle muscle weakness, particularly affecting the pelvic girdle (adductors and flexors of hip).[orpha.net] Showing of 23 30%-79% of people have these symptoms Broad-based gait Wide based walk 0002136 Calf muscle hypertrophy Increased size of calf muscles 0008981 Delayed speech[rarediseases.info.nih.gov]

  • Limb-Girdle Muscular Dystrophy Type 2B

    Erb\'s patient had only shoulder-girdle weakness and atrophy, with sparing of other muscles of the body and a benign disease course compared with that described by Duchenne[checkorphan.org] The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] […] in gross motor skills (e.g., walking, alternating steps on stairs).[now.aapmr.org]

  • Erb Muscular Dystrophy

    Symptoms - Muscular dystrophy limb girdle type 2A- Erb type Muscle weakness is first evident in the shoulder girdle and later in the pelvic girdle.[checkorphan.org] The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] Critical Essential Core Tested Community Questions (19) (SAE13BS.10) A 5-year-old boy has a history of delayed walking and difficulty climbing stairs.[orthobullets.com]

  • Limb-Girdle Muscular Dystrophy Type 2C

    […] dystrophy type 2C (LGMD2C) is a subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a childhood onset of progressive shoulder and pelvic girdle[orpha.net] The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] […] in gross motor skills (e.g., walking, alternating steps on stairs).[now.aapmr.org]

  • Limb-Girdle Muscular Dystrophy Type 2J

    An autosomal recessive degenerative myopathy (OMIM:608807) characterised by progressive weakness of the pelvic and shoulder girdle muscles.[medical-dictionary.thefreedictionary.com] The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] Patient 1 (Figures 2 A–C) exhibited a delay in independent walking until 2.5 years old (y.o.).[frontiersin.org]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy

    […] dystrophy type 2C (LGMD2C) is a subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a childhood onset of progressive shoulder and pelvic girdle[orpha.net] The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] […] in gross motor skills (e.g., walking, alternating steps on stairs).[now.aapmr.org]

Similar symptoms