Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Rev Neurol (Paris) ; 175(3): 194-197, 2019 Mar.
Article in English | MEDLINE | ID: mdl-30314744

ABSTRACT

Familial CCM is a rare entity associated with the mutation of three genes: CCM1 (KRIT1), CCM2 (MGC4607), and CCM3 (PDCD10). We report here the first description of a Tunisian familial CCMs composed of six members. The father and two daughters were affected and symptomatic. The two other kindred were healthy. Surgical treatment was performed in only one affected patient. Molecular analysis of KRIT1, MGC4607 and PDCD10 genes identified a large KRIT1 deletion of the first ten exons. To the best of our knowledge, this large deletion has never been reported before.


Subject(s)
Gene Deletion , Hemangioma, Cavernous, Central Nervous System/genetics , KRIT1 Protein/genetics , Adolescent , Child, Preschool , Consanguinity , Family , Female , Hemangioma, Cavernous, Central Nervous System/diagnosis , Hemangioma, Cavernous, Central Nervous System/pathology , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Tunisia
SELECTION OF CITATIONS
SEARCH DETAIL
...