ML Disorder IV

Crucial
It is feasible that the major title of the report Mucolipidosis IV is not the name you expected. Please examine the basic synonyms specifying to find the alternating name(s) as well as condition neighborhood(s) covered by this report.

Words

  • ML Problem IV
  • ML IV
  • Berman Syndrome
  • Ganglioside Sialidase Deficiency
  • Ganglioside Neuraminidase Deficiency
  • Neuraminidase Shortage
  • Sialolipidosis

Condition Communities

  • None

General Discussion
Mucolipidosis IV is an unusual metabolic problem characterized by intellectual impairment; severe disability in the acquisition of abilities needing the coordination of muscular and also psychological activities (psychomotor retardation); reduced muscular tissue tone (hypotonia); clouding (opacity) of the clear part of the eyes through which light passes (cornea); and progressive weakening of the nerve-rich membrane lining the eyes (retinal weakening). Mucolipidosis IV is acquired as an autosomal recessive hereditary trait and caused by anomalies in the MCOLN1 genetics.

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