Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Case Report: A Case of Moyamoya Syndrome Associated With Multiple Endocrine Neoplasia Type 2A.

Frontiers in endocrinology - 1 Jan 2021

Matano Fumihiro, Murai Yasuo, Watanabe Atsushi, Shirokane Kazutaka, Igarashi Takehito, Shimizu Kazuo, Shimada Takashi, Morita Akio

Abstract excerpt

To the best of our knowledge, we report a case of MEN2A complicated by moyamoya syndrome. A 52-year-old woman presented with vertigo. Magnetic resonance angiography (MRA) revealed bilateral supraclinoid stenosis of the internal carotid artery and abnormal moyamoya-like vessels around the basal ganglia. She had a heterozygous variant of RNF213, which is the susceptibility gene for moyamoya disease. She had also...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adenosine Triphosphatases
Share to Adrenal Gland Neoplasms

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Carcinoma, Neuroendocrine

Share to Moyamoya Disease

Share to Multiple Endocrine Neoplasia Type 2a

Share to Pheochromocytoma

Share to Thyroid Neoplasms

Share to Ubiquitin-Protein Ligases

Source

Open in PubMed Open full text

Identifiers

PMID: 34858321
DOI: 10.3389/fendo.2021.703410
PMCID: PMC8632216

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Case Report: A Case of Moyamoya Syndrome Associated With Multiple Endocrine Neoplasia Type 2A.PMID 34858321Read ↗

Multiple endocrine neoplasia 2A with RET mutation p.Cys611Tyr: A case report.Semantic proximity Read ↗

A case of hemichorea in RNF213-related vasculopathy.Semantic proximity Read ↗

Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.Semantic proximity Read ↗

A rare case of primary hyperparathyroidism associated with primary aldosteronism, Hürthle cell thyroid cancer and meningioma.Semantic proximity Read ↗

Multiple endocrine neoplasia-IIb with RET gene mutation p.M918T： A case report.Semantic proximity Read ↗

MEN2B syndrome - paediatric case report.Semantic proximity Read ↗

Pheochromocytoma as the Index Presentation of Multiple Endocrine Neoplasia Type 2B in a Young Woman with New-Onset Diabetes Mellitus: A Case ReportSemantic proximity Read ↗

Multiple endocrine neoplasia type 2A: case report.Semantic proximity Read ↗

Homozygosity for moyamoya disease risk allele leads to moyamoya disease with extracranial systemic and pulmonary vasculopathy.Semantic proximity Read ↗

Pheochromocytomas in Multiple Endocrine Neoplasia Type 2.Semantic proximity Read ↗

Pheochromocytoma as the first manifestation of MEN2A with RET mutation S891A: report of a case.Semantic proximity Read ↗

Catecholamine crisis as a first manifestation of familial bilateral pheochromocytoma caused by RET proto-oncogene mutation in codon C 634R.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.