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42 Possible Causes for Onset of Symptoms in First or Second Decade of Life, Pediatric Disorder, Shoulder Girdle Weakness

  • 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] Other neuromuscular disorders. Weinstein SL, Flynn JM, eds. Lovell and Winter's Pediatric Orthopaedics. 7th ed.[emedicine.medscape.com]

  • Facioscapulohumeral Muscular Dystrophy

    Symptoms Symptom onset usually occurs during the second decade of life, rarely in infancy or adulthood. Facial muscles are affect first.[symptoma.com] Complications of Neuromuscular Disorders. In Epp, Jr., CH & Bowen Jr., Complications in Pediatric Orthopaedic Surgery, 627-630,1995 Tachdjian M.O.[gait.aidi.udel.edu] We report 10 patients (5 familial, 5 sporadic) with facioscapulohumeral muscular dystrophy (FSHD) with onset of facial and shoulder girdle weakness in early infancy.[ncbi.nlm.nih.gov]

  • Limb-Girdle Muscular Dystrophy Type 2L

    […] 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] 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] Limb girdle muscular dystrophy (LGMD) is a progressive muscle degeneration disorder resulting in profound weakness that affects primarily the shoulder and hip muscles.[ashg.org]

  • Muscular Dystrophy-Dystroglycanopathy Type C5

    […] 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] 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] Pediatric EMG became his major clinical research interest. Dr.[books.google.com]

  • Congenital Merosin-Positive Muscular Dystrophy

    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] Diagnosis of pediatric neuromuscular disorders in the era of DNA analysis. Pediatr Neurol 2000;23: 289–300. [19] Engel 73rd AE.[mafiadoc.com] 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]

  • Kearns-Sayre Syndrome

    Interestingly, some neurological items (section III of NPMDS) remained stable: mild myopathy with symmetrical weakness of hip and shoulder girdle unchanged and neuropathy[doi.org] Signs and symptoms [ edit ] Individuals with KSS present initially in a similar way to those with typical CPEO. Onset is in the first and second decades of life.[en.wikipedia.org] […] symptoms in infants, children, and young adults through images of common and unusual presenting features for over 300 pediatric disorders.[euro-libris.ro]

  • Inherited Neuropathy

    He had weakness of the muscles of the proximal left upper limb, particularly the shoulder girdle.[karger.com] Age of onset is in the second and third decades of life and rarely in the first. Recovery is usually complete and begins weeks to months after the onset of symptoms.[emedicine.medscape.com] He was unable to abduct his left shoulder and had weakness on elbow flexion.[karger.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] Nelson Textbook of Pediatrics. 17th ed. Philadelphia, PA: Elsevier Saunders; 2005:2060-9. Ascadi G. Limb-Girdle Muscular Dystrophy. NORD Guide to Rare Disorders.[rarediseases.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] Pediatric EMG became his major clinical research interest. Dr.[books.google.com]

  • 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] Nelson Textbook of Pediatrics. 17th ed. Philadelphia, PA: Elsevier Saunders; 2005:2060-9. Ascadi G. Limb-Girdle Muscular Dystrophy. NORD Guide to Rare Disorders.[rarediseases.org]