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Journals / Eastern Journal of Medicine / 2018 / Cilt: 23 - Sayı: 4

Niemann-pick type b disease diagnosed in the adulthood

SİNAN DEMİRCİOĞLU
CELALETTİN KORKMAZ
HİLAL AKAY ÇİZMECİOĞLU
NECDET POYRAZ
Pages
322–324
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this paper, we presented NPD type B patient who were diagnosed at 41 years old while being followed for years with the diagnosis of interstitial lung disease.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Niemann-Pick disease (NPD) type B is an autosomal recessive liposomal storage disorder.
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Key Findings & Data:NPD type B can present later in life with predominantly visceral symptoms, and has a more favorable prognosis.
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Conclusion & Impact:In this paper, we presented NPD type B patient who were diagnosed at 41 years old while being followed for years with the diagnosis of interstitial lung disease.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Niemann-Pick disease (NPD) type B is an autosomal recessive liposomal storage disorder. NPD type B can present later in life with predominantly visceral symptoms, and has a more favorable prognosis. The natural history of NPD -B is one of progressive hypersplenism and gradual deterioration of pulmonary function. In this paper, we presented NPD type B patient who were diagnosed at 41 years old while being followed for years with the diagnosis of interstitial lung disease.

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Cite This Article

DEMİRCİOĞLU, S., KORKMAZ, C., ÇİZMECİOĞLU, H. A., POYRAZ, N. (2018). Niemann-pick type b disease diagnosed in the adulthood. Eastern Journal of Medicine, Cilt: 23 - Sayı: 4, 322–324. https://ajindex.com/articles/201306

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