Hallerworden — Spatz disease: clinical observation

Results. The article describes a clinical observation of a rare hereditary Hallervorden – Spatz disease (pantothenate kinase-associated neurodegeneration or neurodegeneration with iron accumulation in the brain) with an atypical late form in the terminal stage with a debut in the fourth decade of li...

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Bibliographic Details
Main Authors: L. B. Novikova, K. M. Ziultsle, A. P. Akopyan
Format: Article
Language:Russian
Published: Open Systems Publication 2025-04-01
Series:Лечащий Врач
Subjects:
Online Access:https://journal.lvrach.ru/jour/article/view/1384
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