Lhermitte-Duclos disease: Difference between revisions
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{{SK}} Dysplastic cerebellar gangliocytoma | {{SK}} Dysplastic cerebellar gangliocytoma | ||
== Overview == | == Overview == | ||
== Historical Perspective == | == Historical Perspective == |
Revision as of 17:55, 15 April 2019
Lhermitte-Duclos disease | |
OMIM | 158350 |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Dysplastic cerebellar gangliocytoma
Overview
Historical Perspective
It was described by Jacques Jean Lhermitte and P. Duclos in 1920.
Epidemiology
Lhermitte-Duclos disease is a rare entity; approximately 220 cases of LDD have been reported in medical literature. It's most common in 3. and 4. decade of life.
Classification
Pathophysiology
Causes
Differentiating Xyz from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
Treatment
Etiology
Cowden disease is caused by mutations of PTEN gene.
Clinical signs
Main clinical signs are:
References
External links