Experience of Hereditary Amyloidosis with Rare Variant in Ecuador: Case Reports.
amyloidosis
cardiomyopathy
mutation
polyneuropathy
transthyretin
Journal
Medical sciences (Basel, Switzerland)
ISSN: 2076-3271
Titre abrégé: Med Sci (Basel)
Pays: Switzerland
ID NLM: 101629322
Informations de publication
Date de publication:
21 Oct 2024
21 Oct 2024
Historique:
received:
14
08
2024
revised:
13
10
2024
accepted:
15
10
2024
medline:
25
10
2024
pubmed:
25
10
2024
entrez:
25
10
2024
Statut:
epublish
Résumé
More than approximately 120 transthyretin mutations are known. Their clinical presentation is heterogeneous, as the course of disease onset depends on genetic variation and level of penetrance. They are little known in Ecuador, and some of the reported cases suggest-given analysis of family trees-that they come from a province that is possibly considered endemic. The main objective of this study is to perform a descriptive observational analysis on the presentation of transthyretin amyloidosis in families carrying the p.Ser43Asn gene of the identified index case.
Identifiants
pubmed: 39449414
pii: medsci12040058
doi: 10.3390/medsci12040058
pii:
doi:
Substances chimiques
Prealbumin
0
TTR protein, human
0
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM