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2,734 Possible Causes for Absent Pulp Chambers, Muscular Atrophy

  • Singleton Merten Syndrome

    Atrophy, Scapuloperoneal OMIM:183020 Spinal Muscular Atrophy, Segmental OMIM:253400 Spinal Muscular Atrophy, Type III; SMA3 OMIM:253550 Spinal Muscular Atrophy, Type II;[] Another related syndrome "familial otodentodysplasia" is characterized by the posterior teeth with abnormal morphology, large pulp chambers, short root length compared to[] Spinal muscular atrophy 1 Spinal muscular atrophy Ryukyuan type Spinal muscular atrophy type 1 with congenital bone fractures Spinal muscular atrophy type 2 Spinal muscular[]

  • Peripheral Neuropathy

    Muscular atrophy of hand muscles persisted. Large fibers were involved more extensively than small fibers.[] 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[]

    Missing: Absent Pulp Chambers
  • 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[] muscular dystrophy Spinal muscular atrophy (SMA) Myotonia congenita Myotonic dystrophy Charcot Marie Tooth disease (hereditary sensory motor neuropathy) At the Pediatric[] […] 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[]

    Missing: Absent Pulp Chambers
  • 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.[] Roche has more than a dozen investigational medicines in clinical development for diseases that include multiple sclerosis, Alzheimer’s disease, spinal muscular atrophy, Parkinson[] 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[]

    Missing: Absent Pulp Chambers
  • 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[] KEYWORDS: Lower motor neuron syndrome; Lower motor neuron-onset ALS; PMA; Progressive muscular atrophy[] […] in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts Applies To Duchenne-Aran muscular atrophy Progressive muscular atrophy (pure[]

    Missing: Absent Pulp Chambers
  • Motor Neuron Disease

    Some MNDs, such as ALS and some forms of spinal muscular atrophy, are fatal.[] A somewhat better prognosis is seen in progressive muscular atrophy, where patients live up to 25 years.[] atrophies (NMAs) and compared these patterns to mouse models of neurogenic muscular atrophy.[]

    Missing: Absent Pulp Chambers
  • Hyperthyroidism

    There are several causes of hyperthyroidism. Most often, the entire gland is overproducing thyroid hormone. This is called Graves' disease. Less commonly, a single nodule is responsible for the excess hormone secretion. We call this a "hot" nodule. Thyroiditis (inflammation of the thyroid) can also cause[…][]

    Missing: Absent Pulp Chambers
  • 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[] atrophy (PMA) and spinal muscular atrophies (SMAs) Upper and lower motor neurons - ALS ALS is the most common of the MNDs.[] 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[]

    Missing: Absent Pulp Chambers
  • 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[] BACKGROUND: Informal caregivers of patients with Amyotrophic Lateral Sclerosis (ALS) or Progressive Muscular Atrophy (PMA) face stressful demands due to severe impairments[] 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.[]

    Missing: Absent Pulp Chambers
  • Multifocal Motor Neuropathy

    Abstract Multifocal motor neuropathy (MMN) and progressive muscular atrophy (PMA) are associated with IgM monoclonal gammopathy or the presence IgM anti-GM1-antibodies.[] Monoclonal gammopathy was determined by immunoelectrophoresis and immunofixation in serum from 445 patients with ALS, 158 patients with progressive muscular atrophy (PMA),[] Atrophy?[]

    Missing: Absent Pulp Chambers

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