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

Hereditary transthyretin amyloidosis in multi-ethnic Malaysians.

Neuromuscular disorders : NMD - 1 Jul 2021

Low Soon-Chai, Md Sari Nor Ashikin, Tan Cheng-Yin, Ahmad-Annuar Azlina, Wong Kum-Thong, Law Wan-Chung, Sim Rachel Siew-Hung, Lin Kon-Ping, Shahrizaila Nortina, Goh Khean-Jin

Abstract excerpt

We report the clinical and genetic characteristics of hereditary transthyretin amyloidosis in the multi-ethnic Malaysian population. Subjects with genetically confirmed transthyretin amyloidosis seen between 2001 till August 2020 were included. There were 30 patients and 14 asymptomatic carriers, of which 26 (59.1%) were men. The majority (86.7%) were ethnic Chinese while two (6.7%) each were Malay and Sri Lankan...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Aged

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Amyloid Neuropathies, Familial

Share to Ethnicity

Share to Malaysia

Share to Mutation

Share to Neurologic Examination

Share to Phenotype

Source

Identifiers

PMID: 34059423
DOI: 10.1016/j.nmd.2021.03.008

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hereditary transthyretin amyloidosis in multi-ethnic Malaysians.PMID 34059423Read ↗

Hereditary Transthyretin Amyloidosis- Clinical and Genetic Characteristics of a Multiracial South-East Asian Cohort in Singapore.Semantic proximity Read ↗

Clinical phenotypes and genetic features of hereditary transthyretin amyloidosis patients in China.Semantic proximity Read ↗

Hereditary transthyretin amyloidosis in mainland China: a unicentric retrospective study.Semantic proximity Read ↗

Clinical and genetic profiles of hereditary transthyretin amyloidosis in TaiwanSemantic proximity Read ↗

Genetic phenotypes and clinical characteristics description of hereditary transthyretin patients in ChinaSemantic proximity Read ↗

A Multicenter Study of Hereditary Transthyretin Amyloidosis in ChinaSemantic proximity Read ↗

Canadian Guidelines for Hereditary Transthyretin Amyloidosis Polyneuropathy ManagementSemantic proximity Read ↗

Unique TTR Variants D38A and M13dup Among Korean Patients with Hereditary Transthyretin Amyloidosis: A Retrospective Single-Center Cohort Study.Semantic proximity Read ↗

Hereditary transthyretin amyloidosis: a myriad of factors that influence phenotypic variability.Semantic proximity Read ↗

Hereditary transthyretin amyloidosis: baseline characteristics of patients in the NEURO-TTR trial.Semantic proximity Read ↗

Updates on hereditary transthyretin amyloidosis polyneuropathy.Semantic proximity Read ↗

Hereditary transthyretin amyloidosis: a comprehensive review with a focus on peripheral neuropathySemantic proximity Read ↗

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