Late diagnosis of tuberous sclerosis complex in a 40-year-old female presenting with abdominal pain: a case report.
angiomyolipomas
cortical tubers
facial angiofibromas
lymphangioleiomyomatosis
subependymal tubers
tuberous sclerosis
Journal
Annals of medicine and surgery (2012)
ISSN: 2049-0801
Titre abrégé: Ann Med Surg (Lond)
Pays: England
ID NLM: 101616869
Informations de publication
Date de publication:
Feb 2023
Feb 2023
Historique:
received:
13
10
2022
accepted:
22
12
2022
entrez:
27
2
2023
pubmed:
28
2
2023
medline:
28
2
2023
Statut:
epublish
Résumé
Tuberous sclerosis (TS) is a rare autosomal-dominant neurocutaneous disorder that is characterized by hamartomas affecting a variety of organs, including the brain, heart, kidneys, skin, lungs, and liver. TS can emerge in a wide variety of clinical and phenotypic forms at any age, all with varying degrees of severity, and is brought on by mutations in the tumor suppressor genes
Identifiants
pubmed: 36845801
doi: 10.1097/MS9.0000000000000149
pmc: PMC9949797
doi:
Types de publication
Journal Article
Langues
eng
Pagination
203-207Informations de copyright
© 2023 the Author(s). Published by Wolters Kluwer Health, Inc.
Déclaration de conflit d'intérêts
There are no conflicts of interest among the authors to disclose.
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