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Moya moya disease: a rare cause of ischemic stroke in children: about a case.

Abstract Moya moya disease is an angiogenic disease characterized by the narrowing of the distal internal carotid artery extending to the proximal segments of the middle and anterior cerebral arteries, inducing collateral vessels formation. These vessels come from the collateral parenchymal vessels, the perforating vessels, leptomeningeal vessels and other transdural anastomoses. These collateral vessels have a characteristic appearance on angiography, forming a cloud of smoke: net-like moyamoya. Its etiology is still poorly understood. Moyamoya disease accounts for 10-15% of the causes of stroke, with 2 age peaks at which its occurrence is more frequent: children around 5 years old and adults around 40 years old. Its evolution can be slow with intermittent symptoms or fulminant with fast neurological deterioration. The current data show the role of surgery as the gold standard for the treatment of moyamoya syndrome, in particular in patients with progressive and recurrent symptoms.
PMID
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Authors

Mayor MeshTerms
Keywords

Moya

angio-MRI

angiography

angioscanner

stroke

vasculitis

Journal Title the pan african medical journal
Publication Year Start



 

PMID- 29599890
OWN - NLM
STAT- MEDLINE
DCOM- 20180405
LR  - 20180405
IS  - 1937-8688 (Electronic)
VI  - 28
DP  - 2017
TI  - [Moya moya disease: a rare cause of ischemic stroke in children: about a case].
PG  - 192
LID - 10.11604/pamj.2017.28.192.8740 [doi]
AB  - Moya moya disease is an angiogenic disease characterized by the narrowing of the 
      distal internal carotid artery extending to the proximal segments of the middle
      and anterior cerebral arteries, inducing collateral vessels formation. These
      vessels come from the collateral parenchymal vessels, the perforating vessels,
      leptomeningeal vessels and other transdural anastomoses. These collateral vessels
      have a characteristic appearance on angiography, forming a cloud of smoke:
      net-like moyamoya. Its etiology is still poorly understood. Moyamoya disease
      accounts for 10-15% of the causes of stroke, with 2 age peaks at which its
      occurrence is more frequent: children around 5 years old and adults around 40
      years old. Its evolution can be slow with intermittent symptoms or fulminant with
      fast neurological deterioration. The current data show the role of surgery as the
      gold standard for the treatment of moyamoya syndrome, in particular in patients
      with progressive and recurrent symptoms.
FAU - Chibli, Radia
AU  - Chibli R
AD  - Service de Neuroradiologie, Hopital des Specialites, Rabat, Maroc.
FAU - Omor, Youssef
AU  - Omor Y
AD  - Service de Neuroradiologie, Hopital des Specialites, Rabat, Maroc.
FAU - Sebbouba, Nadir Slimani
AU  - Sebbouba NS
AD  - Service de Neuroradiologie, Hopital des Specialites, Rabat, Maroc.
FAU - Hassani, Moulay Rachid El
AU  - Hassani MRE
AD  - Service de Neuroradiologie, Hopital des Specialites, Rabat, Maroc.
FAU - Jiddane, Mohamed
AU  - Jiddane M
AD  - Service de Neuroradiologie, Hopital des Specialites, Rabat, Maroc.
FAU - Fikri, Meriem
AU  - Fikri M
AD  - Service de Neuroradiologie, Hopital des Specialites, Rabat, Maroc.
LA  - fre
PT  - Case Reports
PT  - Journal Article
TT  - Moya moya: etiologie rare d'accident vasculaire cerebral ischemique chez
      l'enfant: a propos d'un cas.
DEP - 20171101
PL  - Uganda
TA  - Pan Afr Med J
JT  - The Pan African medical journal
JID - 101517926
SB  - IM
MH  - Brain Ischemia/*etiology/pathology
MH  - Carotid Artery, Internal/pathology
MH  - Child, Preschool
MH  - Humans
MH  - Male
MH  - Moyamoya Disease/*complications/physiopathology
MH  - Stroke/*etiology/pathology
PMC - PMC5871250
OTO - NOTNLM
OT  - Moya
OT  - angio-MRI
OT  - angiography
OT  - angioscanner
OT  - stroke
OT  - vasculitis
EDAT- 2018/03/31 06:00
MHDA- 2018/04/06 06:00
CRDT- 2018/03/31 06:00
PHST- 2015/12/28 00:00 [received]
PHST- 2016/03/08 00:00 [accepted]
PHST- 2018/03/31 06:00 [entrez]
PHST- 2018/03/31 06:00 [pubmed]
PHST- 2018/04/06 06:00 [medline]
AID - 10.11604/pamj.2017.28.192.8740 [doi]
AID - PAMJ-28-192 [pii]
PST - epublish
SO  - Pan Afr Med J. 2017 Nov 1;28:192. doi: 10.11604/pamj.2017.28.192.8740.
      eCollection 2017.