MyMedR
Advanced
  • Browse
  • Help
  • Login
Advanced

Familial lichen amyloidosis. Report of 19 cases in 4 generations of a Chinese family in Malaysia

Rajagopalan K , Tay CH
Br J Dermatol, 1972 Aug;87(2):123-9.
PMID: 5057380 DOI: 10.1111/j.1365-2133.1972.tb16186.x

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

MeSH terms
  • Adolescent
  • Adult
  • Age Factors
  • Aged
  • Amyloidosis/genetics*
  • Female
  • Genes, Dominant
  • Humans
  • Male
  • Middle Aged
  • Pedigree
  • Puberty
  • Sex Factors
  • Skin Diseases/genetics*
Similar publications
  • MicroRNA expression profile of a Malaysian Bajau family with familial mitochondrial neurogastrointestinal encephalomyopathy
  • Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study
  • Investigation of a PAX6 gene mutation in a Malaysian family with congenital aniridia
  • Cerebrotendinous xanthomatosis with cholestanolaemia--involvement of five individuals in a Malay family
  • Hidrotic ectodermal dysplasia: study of a large Chinese pedigree
  • Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families
  • Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study
  • Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk
  • Loss-of-Function Myeloperoxidase Mutations Are Associated with Increased Neutrophil Counts and Pustular Skin Disease
  • APOE ε4 and the Influence of Sex, Age, Vascular Risk Factors, and Ethnicity on Cognitive Decline
  • Related publications on PubMed
Copyright © 2026 MyMedR. Developed by Rakit.

* MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.