Create issue ticket

241 Possible Causes for Onset Usually in First or Second Decade, Persistent Notochordal Canal

  • Distal Hereditary Motor Neuropathy Type 1

    In general, in most CMT subtypes onset is usually during the first or second decade of life. Both motor and sensory nerve functions are affected.[academlib.com] notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] […] syndrome SLC35A1-CDG SLC35A2-CDG SSR4-CDG STT3A-CDG STT3B-CDG SURF1-related Charcot-Marie-Tooth disease type 4 Sacral agenesis-abnormal ossification of the vertebral bodies-persistent[se-atlas.de]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2J

    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] notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] : Expression in either male or female sex Onset usually in the late first or second decade of life (but also middle age) Usually autosomal recessive and less frequently autosomal[emedicine.medscape.com]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2R

    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] notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] LGMD1C (caveolinopathy) Onset is usually in the first or second decade, but it may manifest into early adulthood.[emedicine.medscape.com]

  • Alpha-B Crystallinopathy

    LGMD1C (caveolinopathy) Onset is usually in the first or second decade, but it may manifest into early adulthood.[emedicine.medscape.com] notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] Atrioventricular (AV) block progresses from first degree to complete. Dilated cardiomyopathy and ventricular arrhythmias may also be present.[emedicine.medscape.com]

  • X-linked Parkinsonism-Spasticity Syndrome

    […] of the disease, with the mean usually within the first or second decade.[jnnp.bmj.com] There has been no evidence to suggest anticipation of age at onset in successive generations.[jnnp.bmj.com] […] the SPG3 gene on chromosome14q11.2-q24.3 has been narrowed to a 7 cM region. 88 90 95-97 Among the five families there does seem to be a trend to a relatively early age at onset[jnnp.bmj.com]

    Missing: Persistent Notochordal Canal
  • Familial Recurrent Peripheral Facial Palsy

    notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] […] syndrome SLC35A1-CDG SLC35A2-CDG SSR4-CDG STT3A-CDG STT3B-CDG SURF1-related Charcot-Marie-Tooth disease type 4 Sacral agenesis-abnormal ossification of the vertebral bodies-persistent[se-atlas.de]

    Missing: Onset Usually in First or Second Decade
  • Lafora Disease

    Survival is short, less than 10 years after onset, which is usually in the first half of the second decade of life.[medlink.com]

    Missing: Persistent Notochordal Canal
  • Generalized Clonic or Tonic-Clonic Seizures

    The seizures are usually well controlled with medication. Age at Onset: 5 to 40 years (peak 11-23 years); 80% have their first GTCS in the second decade of life.[pennsw.com.au]

    Missing: Persistent Notochordal Canal
  • Essential Tremor

    Studies have shown that there is a bimodal distribution of age at onset with peaks in the second and sixth decades.[bcm.edu] Patients usually first become aware of the tremor when they are holding newspapers or utensils or when reaching for objects.[bcm.edu]

    Missing: Persistent Notochordal Canal
  • Familial Visceral Myopathy

    Disease onset is usually in the first or second decade of life, and the illness slowly progresses until usually all ocular motility is lost.[bioportfolio.com]

    Missing: Persistent Notochordal Canal

Further symptoms

Similar symptoms