Nasu-Hakola disease as suspected cause for bone disease and dementia

Maryam Sahebari1, Bita Abbasi, Ali Akhondpour Manteghi

  • 1From the *Rheumatic Diseases Research Center (RDRC), School of Medicine, †Radiology Department, Ghaem Hospital, School of Medicine, and ‡Avicenna Hospital, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Islamic Republic of Iran.

Insights

Nasu-Hakola disease, a rare genetic condition, causes bone fractures and presenile dementia. This case highlights the importance of considering this diagnosis in young men with these symptoms.

Area of Science:

  • Neurology
  • Genetics
  • Orthopedics

Background:

  • Investigating progressive dementia and multiple bone fractures in a young man.
  • Basal ganglia calcifications complicated differential diagnoses, including hypoparathyroidism.

Observation:

  • A patient presented with progressive dementia and multiple bone fractures.
  • Brain CT revealed basal ganglia calcifications.

Findings:

  • Literature search identified Nasu-Hakola disease (polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy).
  • This rare genetic disorder is marked by pathological fractures, bone lesions, and presenile dementia.

Implications:

  • This case expands the understanding of Nasu-Hakola disease presentation.
  • Highlights the need for early diagnosis of this rare genetic condition.

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