Timothy syndrome

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Name:
Timothy syndrome
Description:
A rare, multiple congenital anomalies syndrome with cardiac involvement as a major feature characterized by QT prolongation, congenital heart defects, syndactyly, facial dysmorphism and neurodevelopmental features. There are three clinical phenotypes recognized, the classical types that present with a prolonged QT interval and either with (TS1) or without (TS2) cutaneous syndactyly of fingers and toes. The atypical form (ATS) causes multi-system health concerns but not necessarily with prolonged QT.
ORPHAcode:
65283
Synonyms:
LQT8
Long QT syndrome type 8
Long QT syndrome-syndactyly syndrome
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
01 Aug 2021 - 06:46