Pelizaeus-Merzbacher sclerosis
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Pelizaeus-Merzbacher disease — Pel·i·zae·us Merz·bach·er disease .pel ēt sā əs merts .bäk ər n a familial degenerative disease of the central nervous system that is characterized by slowly progressive demyelination of white matter resulting in mental deterioration and the… … Medical dictionary
Список наследственных заболеваний — Список генетических заболеваний Основные статьи: наследственные заболевания, Наследственные болезни обмена веществ, Ферментопатия. В большинстве случаев приведен также код, указывающий на тип мутации и связанные с ней хромосомы. См. также система … Википедия
Disease — Illness or sickness often characterized by typical patient problems (symptoms) and physical findings (signs). Disruption sequence: The events that occur when a fetus that is developing normally is subjected to a destructive agent such as the… … Medical dictionary
List of diseases (P) — A list of diseases in the English Wikipedia.DiseasesTOC PaPac Pal* Pachydermoperiostosis * Pachygyria * Pachyonychia congenita Jackson Lawler type * Pacman dysplasia * Paes Whelan Modi syndrome * Paget disease extramammary * Paget disease… … Wikipedia
Nystagmus — Horizontal optokinetic nystagmus, a normal (physiological) form of nystagmus ICD 10 H55, H81.4 … Wikipedia
List of neurological disorders — This is a list of major and frequently observed neurological disorders (e.g., Alzheimer s disease), symptoms (e.g., back pain), signs (e.g., aphasia) and syndromes (e.g., Aicardi syndrome). Contents: Top · 0–9 A B C D E F G H I J K L M N O P … Wikipedia
The Myelin Project — is an international scientific research organization aimed at accelerating clinical and translational research focused on myelin repair and to regenerate the nerve s myelin sheath, a process called remyelination destroyed in a host of diseases… … Wikipedia
Charcot–Marie–Tooth disease — Charcot Marie Tooth disease Classification and external resources The foot of a person with Charcot Marie Tooth. The lack of muscle, a high arch, and claw toes are signs of the genetic disease. ICD 10 … Wikipedia
Laminopathy — Normal nuclear lamina (a and b) and mutant nuclear lamina (c and d) from a patient with HGPS, visualized by immunofluorescence note the irregular and bumpy shape of the laminopathic nuclei[1] Laminopathies are a group of rare genetic disorders… … Wikipedia
X-linked lymphoproliferative disease — Classification and external resources ICD 10 D82.3 OMIM 308240 300635 … Wikipedia
