A Case of Neurofibromatosis type 1 with Moya Moya Disease

SJ Bhuiyan

PULSE · 2018-yil

Annotatsiya

A 5 years old boy with multiple café au lait spots came with intermittent weakness of the right side of the body and seizures. The child had global developmental delay. His MRI and MRA showed thickening of the optic nerves, abnormal signal in multiple areas of the brain with non-visuation of the left middle cerebral artery. The child was diagnosed to have neurofibromatosis type 1 with seizures with bilateral optic glioma with Moya Moya disease.Pulse Vol.10 January-December 2017 p.34-37

Maqola ma’lumotlari
MualliflarSJ Bhuiyan
JurnalPULSE
NashriyotPROFI университетининг
ISSN2074-1855, 2235-8668
Nashr sanasi2018-10-19
Jild10
Son1
Betlar34-37
TilIngliz
Ilmiy sohaPsixologiya
DOI10.3329/pulse.v10i1.38610
Indeksga qo‘shilgan2026-09-02

DOI: 10.3329/pulse.v10i1.38610 · Maqolaning asl sahifasi

Ilmiy soha

Psixologiya

Iqtibos keltirish

APASJ Bhuiyan (2018). A Case of Neurofibromatosis type 1 with Moya Moya Disease. PULSE, 10(1), 34-37. https://doi.org/10.3329/pulse.v10i1.38610
GOST (OAK)SJ Bhuiyan A Case of Neurofibromatosis type 1 with Moya Moya Disease // PULSE. – 2018. – T. 10, № 1. – P. 34-37. – DOI: 10.3329/pulse.v10i1.38610.
MLASJ Bhuiyan. “A Case of Neurofibromatosis type 1 with Moya Moya Disease.” PULSE, 10(1), 34-37, 2018. https://doi.org/10.3329/pulse.v10i1.38610
ChicagoSJ Bhuiyan. “A Case of Neurofibromatosis type 1 with Moya Moya Disease.” PULSE, 10(1), 34-37 (2018). https://doi.org/10.3329/pulse.v10i1.38610
HarvardSJ Bhuiyan (2018) ‘A Case of Neurofibromatosis type 1 with Moya Moya Disease’, PULSE, 10(1), 34-37. https://doi.org/10.3329/pulse.v10i1.38610
BibTeX
@article{sjbhuiyan2018,
  title = {A Case of Neurofibromatosis type 1 with Moya Moya Disease},
  author = {SJ Bhuiyan},
  journal = {PULSE},
  year = {2018},
  volume = {10},
  number = {1},
  pages = {34-37},
  doi = {10.3329/pulse.v10i1.38610},
  url = {https://doi.org/10.3329/pulse.v10i1.38610}
}

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