Ring chromosome 14 syndrome: what the dentist should know to manage children with r(14) effec-tively
Introduction: Ring chromosome 14 syndrome, or r(14), is a rare genetic disorder characterized by distinctive facial features, intractable epilepsy, delayed development, intellectual disability, and autism spectrum disorder. With less than 100 documented cases worldwide, the disease is not well known...
Main Authors: | Athena E. Ivanoff, Chris S. Ivanoff |
---|---|
Format: | Article |
Language: | English |
Published: |
Pensoft Publishers
2023-02-01
|
Series: | Folia Medica |
Subjects: | |
Online Access: | https://foliamedica.bg/article/71784/download/pdf/ |
Similar Items
-
Complete trisomy 14 mosaicism: first live-born case in Korea
by: Yun Jung Hur, et al.
Published: (2012-10-01) -
The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chromosomes
by: Peining Li, et al.
Published: (2022-10-01) -
Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes
by: Angela Peron, et al.
Published: (2020-12-01) -
Epilepsy and ring chromosome 20: case report
by: Gomes Marleide da Mota, et al.
Published: (2002-01-01) -
Synteny of human chromosomes 14 and 15 in the platyrrhines (Primates, Platyrrhini)
by: Cristiani Gifalli-Iughetti, et al.
Published: (2009-01-01)