Create issue ticket

18 Possible Causes for Biceps Brachii Atrophy, Onset of Symptoms in First or Second Decade of Life, Shoulder Girdle Weakness

  • 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] LGMD 2L is characterized by late-onset (mean age 35) proximal weakness with prominent asymmetrical quadriceps femoris and biceps brachii atrophy.[egl-eurofins.com]

  • Limb-Girdle Muscular Dystrophy Type 2A

    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] The patients had early asymmetric muscle involvement characterized by prominent biceps brachii atrophy with sparing of the knee extensors.[ncbi.nlm.nih.gov] Many pathogenic mutations have been identified in calpain3, encoded by the CAPN3 gene, which leads to weakness of the pelvic and shoulder girdle muscles.[uniprot.org]

  • Limb-Girdle Muscular Dystrophy

    Abstract Limb-girdle muscular dystrophies (LGMD) are a highly heterogeneous group of genetic myopathies characterized by progressive proximal pelvic and/or shoulder girdle[ncbi.nlm.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] The patients had early asymmetric muscle involvement characterized by prominent biceps brachii atrophy with sparing of the knee extensors.[ncbi.nlm.nih.gov]

  • Facioscapulohumeral Muscular Dystrophy

    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] Symptoms Symptom onset usually occurs during the second decade of life, rarely in infancy or adulthood. Facial muscles are affect first.[symptoma.com] Physical examination revealed marked bilateral atrophy at biceps brachii, bilateral scapular winging, some asymmetrical weakness at tibialis anterior and peroneal muscles,[ncbi.nlm.nih.gov]

  • Secondary Myopathy

    Commonly, pelvic girdle muscles are involved before and much more severely than shoulder girdle muscles.[clevelandclinicmeded.com] Childhood onset weakness, contractures, and early cardiac involvement. Symptoms usually develop in the first or second decade of life.[sites.google.com] , with the pelvic girdle musculature nearly always being more severely affected than the shoulder girdle muscles (presentation with shoulder girdle weakness is unusual).[jnnp.bmj.com]

  • Distal Myopathy Type 3

    Commonly, pelvic girdle muscles are involved before and much more severely than shoulder girdle muscles.[clevelandclinicmeded.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] […] of the quadriceps femoris and biceps brachii.[sites.google.com]

  • Emery-Dreifuss Muscular Dystrophy Type 2

    - can't whistle, Shoulder girdle weakness, & Variable hearing loss Fascioscapulohumeral (FSHMD) Rigidity of neck and spine In FSHMD the associated facial weakness does not[quizlet.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] brachii) and case 2 (right m bicepsbrachii)Case 1 Case 2Fiber size variation Type-I atrophy Type-II hypertrophy Group atrophy ( ) Fiber type grouping Increased internal nuclei[docslide.com.br]

  • Polyglucosan Body Myopathy Type 2

    Limb-girdle muscular dystrophy is characterized by weakness and wasting predominately of the hips, shoulders, and proximal extremity muscles.[mayomedicallaboratories.com] Childhood onset weakness, contractures, and early cardiac involvement. Symptoms usually develop in the first or second decade of life.[sites.google.com] Most patients manifest slowly progressive, hip girdle, shoulder girdle, and/or hand and leg muscle weakness.[genecards.org]

  • Autosomal Dominant Myoglobinuria

    Commonly, pelvic girdle muscles are involved before and much more severely than shoulder girdle muscles.[clevelandclinicmeded.com] A late-onset myotubular myopathy has been also reported, which presents with milder symptoms during childhood that worsen after the first or second decade of life and that[intechopen.com] […] of the quadriceps femoris and biceps brachii.[sites.google.com]

  • Congenital Myopathy with Excess of Thin Filaments

    Tip-toe is not possible Over time the pattern is one of proximal hip-girdle weakness followed by shoulder-girdle weakness.[sites.google.com] Childhood onset weakness, contractures, and early cardiac involvement. Symptoms usually develop in the first or second decade of life.[sites.google.com] […] of the quadriceps femoris and biceps brachii.[sites.google.com]