Create issue ticket

3,125 Possible Causes for Muscular Atrophy, Onset of Symptoms in the Fourth to Sixth Decade of Life

  • Charcot-Marie-Tooth Disease Type 2S

    atrophy with respiratory distress (sequence analysis of IGHMBP2 gene) Charcot-Marie-Tooth disease (disease exome based NGS panel for 43 genes) Spinal muscular atrophy (NGS[cgcgenetics.com] Clinical and electrophysiological data Limbs Onset of peripheral neuropathic symptoms was between the fourth and the sixth decades of life in five out of the seven patients[jnnp.bmj.com] Neuropathy With Respiratory Failure Spinal Muscular Atrophy With Respiratory Distress 1 Spinal Muscular Atrophy, Diaphragmatic DSMA1 DHMN6 HMN VI HMN6 SIANRF SMARDI 604320[ukgtn.nhs.uk]

  • Peripheral Neuropathy

    Muscular atrophy of hand muscles persisted. Large fibers were involved more extensively than small fibers.[ncbi.nlm.nih.gov] Boulis works on novel treatments for several nerve disorders, including Amyotrophic Lateral Sclerosis (ALS, also known as Lou Gehrig's disease) and Spinal Muscular Atrophy[emoryhealthcare.org]

    Missing: Onset of Symptoms in the Fourth to Sixth Decade of Life
  • Polyneuropathy

    Neuronal Peroneal Muscular Atrophy (HMSN II) Autosomal dominant inheritance is also the case with HMSN II.[lecturio.com] Ciliary neurotrophic factor-induced sprouting preserves motor function in a mouse model of mild spinal muscular atrophy. Hum. Mol.[doi.org] Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography .[go.nature.com]

    Missing: Onset of Symptoms in the Fourth to Sixth Decade of Life
  • Carpal Tunnel Syndrome

    Motor complaints relate to thenar muscular weakness and atrophy.[ncbi.nlm.nih.gov] (particularly peroneal muscular atrophy) resulting in foot dorsiflexor weakness, foot drop, and secondary steppage gait.[doi.org] Charcot–Marie–Tooth disease is highly variable in presentation but is characterized by distal symmetric polyneuropathy, 9 with slowly progressive distal muscle weakness and atrophy[doi.org]

    Missing: Onset of Symptoms in the Fourth to Sixth Decade of Life
  • Muscular Dystrophy

    Distal muscular dystrophies are a group of inherited primary muscle disorders showing progressive weakness and atrophy preferentially in the hands, forearm, lower legs, or[ncbi.nlm.nih.gov] muscular dystrophy Spinal muscular atrophy (SMA) Myotonia congenita Myotonic dystrophy Charcot Marie Tooth disease (hereditary sensory motor neuropathy) At the Pediatric[ynhh.org] […] with: Friedreich's ataxia Myasthenia gravis Spinal muscular atrophy Appointments and Location (804) 828-CHOR (2467) Children's Pavilion - Level 3, Pod B ›› Meet the Team[chrichmond.org]

    Missing: Onset of Symptoms in the Fourth to Sixth Decade of Life
  • Primary Progressive Multiple Sclerosis

    In late-stage Roche, they have treatments that are being tested for Alzheimer’s disease, Autism, and for Spinal Muscular Atrophy.[mdmag.com] Roche has more than a dozen investigational medicines in clinical development for diseases that include multiple sclerosis, Alzheimer’s disease, spinal muscular atrophy, Parkinson[finance.yahoo.com] 脊髄性筋萎縮症 Spinal muscular atrophy, SMA Type I 脊髄性筋萎縮症(SMA Type I) 1 HPS0158 HPS0159 Spinal muscular atrophy, SMA Type II 脊髄性筋萎縮症(SMA Type II) 1 不要 有 HPS1391 HPS1392 HPS1393[cell.brc.riken.jp]

    Missing: Onset of Symptoms in the Fourth to Sixth Decade of Life
  • Progressive Muscular Atrophy

    The name "spinal muscular atrophy" is ambiguous as it refers to any of various spinal muscular atrophies, including the autosomal recessive spinal muscular atrophy caused[en.wikipedia.org] KEYWORDS: Lower motor neuron syndrome; Lower motor neuron-onset ALS; PMA; Progressive muscular atrophy[ncbi.nlm.nih.gov] Our electrophysiological data in patients recently diagnosed with sporadic progressive muscular atrophy are consistent with widespread LMN loss.[ncbi.nlm.nih.gov]

    Missing: Onset of Symptoms in the Fourth to Sixth Decade of Life
  • Motor Neuron Disease

    Some MNDs, such as ALS and some forms of spinal muscular atrophy, are fatal.[ninds.nih.gov] A somewhat better prognosis is seen in progressive muscular atrophy, where patients live up to 25 years.[symptoma.com] It is a rare form of muscular atrophy leading to weakness.[imnda.ie]

    Missing: Onset of Symptoms in the Fourth to Sixth Decade of Life
  • Primary Lateral Sclerosis

    This locus had not been implicated in ALS or in hereditary spastic parapareses, spinal muscular atrophy, or spinal and bulbar muscular atrophy. [7] A genetically mediated[emedicine.com] atrophy (PMA) and spinal muscular atrophies (SMAs) Upper and lower motor neurons - ALS ALS is the most common of the MNDs.[emedicine.com] The traditional classification of MNDs is according to the affected cell types, as follows: Upper motor neurons alone - PLS Lower motor neurons alone - Progressive muscular[emedicine.com]

    Missing: Onset of Symptoms in the Fourth to Sixth Decade of Life
  • Amyotrophic Lateral Sclerosis

    The patients were a 54-year-old man with progressive muscular atrophy who underwent removal of internal fixators in the arm and leg, and a 66-year-old woman with amyotrophic[ncbi.nlm.nih.gov] BACKGROUND: Informal caregivers of patients with Amyotrophic Lateral Sclerosis (ALS) or Progressive Muscular Atrophy (PMA) face stressful demands due to severe impairments[ncbi.nlm.nih.gov] Excluding lower motor neuron FA and FL cases, progressive muscular atrophy comprised 4% of the sample and had a prognosis similar to typical limb onset ALS.[ncbi.nlm.nih.gov]

    Missing: Onset of Symptoms in the Fourth to Sixth Decade of Life

Further symptoms

Similar symptoms