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Published on: December 18, 2016
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.
Abstract:
Progressive dementia in conjunction with multiple bone fractures in a previously healthy young man led to the investigation of the underlying cause. The differential diagnoses (most importantly hypoparathyroidism) were limited given basal ganglia calcifications on the brain computed tomographic scan. Electronic search of the key words basal ganglia calcification, osteoporosis, and dementia revealed a rare condition termed Nasu-Hakola disease or polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy. This very rare and potentially fatal genetic disease is characterized by pathological fractures, multiple lytic bone lesions, and presenile dementia. We report an Iranian patient with this disease and a review of the literature.
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