Create issue ticket

3,082 Possible Causes for Absent Pulp Chambers, Allelic to Dentin Dysplasia Type 2, 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;[informatics.jax.org] Another related syndrome "familial otodentodysplasia" is characterized by the posterior teeth with abnormal morphology, large pulp chambers, short root length compared to[indjos.com] 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[personalizedcause.com]

    Missing: Allelic to Dentin Dysplasia Type 2
  • Dentinogenesis Imperfecta Type 1

    […] root canals Absent root tooth Amber colored teeth Misaligned teeth Recurring dental abscess Blue sclera Enamel separation from the ivory Very small pulp chambers Very small[medicalsubstance.com] Symptoms of Dentinogenesis imperfecta Type I It is characterized by several tooth structure abnormalities, some of which include: Bluish-gray teeth Bulbous teeth crowns Absent[medicalsubstance.com]

    Missing: Muscular Atrophy
  • 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: Absent Pulp Chambers Allelic to Dentin Dysplasia Type 2
  • 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: Absent Pulp Chambers Allelic to Dentin Dysplasia Type 2
  • 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: Absent Pulp Chambers Allelic to Dentin Dysplasia Type 2
  • 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: Absent Pulp Chambers Allelic to Dentin Dysplasia Type 2
  • 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: Absent Pulp Chambers Allelic to Dentin Dysplasia Type 2
  • 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] […] in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts Applies To Duchenne-Aran muscular atrophy Progressive muscular atrophy (pure[icd9data.com]

    Missing: Absent Pulp Chambers Allelic to Dentin Dysplasia Type 2
  • 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: Absent Pulp Chambers Allelic to Dentin Dysplasia Type 2
  • 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: Absent Pulp Chambers Allelic to Dentin Dysplasia Type 2

Similar symptoms