Create issue ticket

44 Possible Causes for Mild Facial Weakness, 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] May have mild facial weakness. May have cardiac involvement; there is no respiratory involvement. May have normal CK.[patient.info]

  • 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] facial weakness Knee contractures Ankle contractures Hip contractures Spine deformity High arched palate Causes - Muscular dystrophy- congenital- merosin-positive Not supplied[checkorphan.org]

  • Limb-Girdle Muscular Dystrophy Type 1E

    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] […] bulbar/facial weakness.[emedicine.medscape.com]

  • 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] Affected individuals develop weakness of the lower limbs that may be mild or severe. Weakness of facial muscles may also occur.[rarediseases.org]

  • Limb-Girdle Muscular Dystrophy Type 2E

    shoulder-girdle muscle weakness, particularly affecting the pelvic girdle (adductors and flexors of hip).[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] May have mild facial weakness. May have cardiac involvement; there is no respiratory involvement. May have normal CK.[patient.info]

  • 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] May have mild facial weakness. May have cardiac involvement; there is no respiratory involvement. May have normal CK.[patient.info]

  • 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] May have mild facial weakness. May have cardiac involvement; there is no respiratory involvement. May have normal CK.[patient.info]

  • 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] The patient presented with mild facial weakness, humeral poly-hill sign, scapular winging, peroneal weakness, drop foot, pes cavus, and myoclonic epilepsy.[ncbi.nlm.nih.gov]

  • 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] May have mild facial weakness. May have cardiac involvement; there is no respiratory involvement. May have normal CK.[patient.info]

  • Limb-Girdle Muscular Dystrophy Type 2Q

    […] 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] May have mild facial weakness. May have cardiac involvement; there is no respiratory involvement. May have normal CK.[patient.info]