Neuronal intranuclear inclusion disease

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Alternate names[edit | edit source]

NIID; Neuronal intranuclear hyaline inclusion disease

Definition[edit | edit source]

Neuronal intranuclear inclusion disease (NIID) is a slowly progressive, neurodegenerative disease.

Cause[edit | edit source]

In many families, neuronal intranuclear inclusion disease (NIID) is caused by a genetic change in the NOTCH2NLC gene.

Inheritance[edit | edit source]

Autosomal dominant pattern, a 50/50 chance.
  • Neuronal intranuclear inclusion disease (NIID) appears to be inherited in an autosomal dominant pattern in families.
  • In some cases, a person will be the first in their family to develop the condition due to new genetic changes in the NOTCH2NLC gene that result in NIID.

Onset[edit | edit source]

Signs and symptoms may begin anywhere from infancy to late adulthood, and can vary from person to person. In most cases, the disease begins in childhood.

Signs and symptoms[edit | edit source]

Diagnosis[edit | edit source]

  • The rectal and skin biopsy had proved helpful in antemortem diagnosis.[1].
  • The diagnostic armamentarium by showing the presence of intranuclear inclusions in smooth muscle cells of the muscle.
  • Hence, a high degree of suspicion, magnetic resonance imaging features, with nerve/muscle/skin biopsy can help in diagnosis of NIID.

Treatment[edit | edit source]

Currently there is no treatment that cures or slows the progression of NIID, but medications that help control symptoms may improve quality of life. While the disease is ultimately fatal, life expectancy can range significantly, from one year to several decades after the diagnosis.


References[edit | edit source]

  1. Yadav N, Raja P, Shetty SS, Jitender S, Prasad C, Kamble NL, Mahadevan A, M N. Neuronal Intranuclear Inclusion Disease: A Rare Etiology for Rapidly Progressive Dementia. Alzheimer Dis Assoc Disord. 2019 Oct-Dec;33(4):359-361. doi: 10.1097/WAD.0000000000000312. PMID: 31094708.

NIH genetic and rare disease info[edit source]

Neuronal intranuclear inclusion disease is a rare disease.


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