A Sporadic Case of Late Onset Transthyretin Related Familial Amyroid Cardiomyopathy (TTR-FAC) Preceded by Atrioventricular Conduction Disturbance

2016 ◽  
Vol 22 (9) ◽  
pp. S219
Author(s):  
Koichiro Takayama ◽  
Hiroshi Sakai ◽  
Minoru Horie
Keyword(s):  
Late Onset ◽  
Sporadic Case ◽  
Atrioventricular Conduction ◽  
Conduction Disturbance

scholarly journals Atrial tachycardia, atrioventricular conduction disturbance and right heart failure years after removal of a cardiac hydatid cyst

2017 ◽  
Vol 3 (5) ◽  
Author(s):  
Christos – Konstantinos Antoniou ◽  
Petros Arsenos ◽  
Nikos Apostolopoulos ◽  
Polychronis Dilaveris ◽  
Skevos Sideris ◽  
...  
Keyword(s):  
Heart Failure ◽  
Hydatid Cyst ◽  
Atrial Tachycardia ◽  
Right Heart Failure ◽  
Atrioventricular Conduction ◽  
Conduction Disturbance ◽  
Right Heart

scholarly journals Arrhythmogenic right ventricular dysplasia with sick sinus syndrome and atrioventricular conduction disturbance.

1990 ◽  
Vol 31 (3) ◽  
pp. 417-423 ◽  
Author(s):  
Akihiko NOGAMI ◽  
Susumu ADACHI ◽  
Jun-ichi NITTA ◽  
Koichi TANIGUCHI ◽  
Fumiaki MARUMO ◽  
...  
Keyword(s):  
Right Ventricular ◽  
Sick Sinus Syndrome ◽  
Arrhythmogenic Right Ventricular Dysplasia ◽  
Atrioventricular Conduction ◽  
Conduction Disturbance ◽  
Right Ventricular Dysplasia

Arrhythmogenic right ventricular dysplasia associated with atrioventricular conduction disturbance

1983 ◽  
Vol 52 (7) ◽  
pp. 909-912 ◽  
Author(s):  
Lee B. Beerman ◽  
James R. Zuberbuhler ◽  
William H. Neches ◽  
Donald R. Fischer ◽  
Frederick J. Fricker ◽  
...  
Keyword(s):  
Right Ventricular ◽  
Arrhythmogenic Right Ventricular Dysplasia ◽  
Atrioventricular Conduction ◽  
Conduction Disturbance ◽  
Right Ventricular Dysplasia

scholarly journals A SPORADIC CASE OF ERYTHROKERATODERMIA VARIABILIS IN AN ADULT

2019 ◽  
pp. 1-2
Author(s):  
Anupama Wahengbam
Keyword(s):  
Late Onset ◽  
Sporadic Case ◽  
Diverse Group

Erythrokeratoderma are diverse group of genodermatosis affecting keratinization under which, Erythrokeratodermia Variabilis ( EKV) was first described in 1925 by Mendes da Costa. Our patient is a 48 year old male presenting clinically with EKV Mendes Da Costa, hyperkeratotic subtype with the histopathology supportive of the diagnosis. We are reporting for its rarity and due to its late onset in our patient and also for the sporadic nature of this particular case of EKV.

A sporadic case of late-onset familial amyloid polyneuropathy with Bence-Jones proteinuria

1999 ◽  
Vol 246 (8) ◽  
pp. 726-727 ◽  
Author(s):  
M. Yamada ◽  
A. Nonaka ◽  
T. Kamata ◽  
T. Furuya ◽  
H. Mizusawa
Keyword(s):  
Late Onset ◽  
Sporadic Case ◽  
Familial Amyloid Polyneuropathy ◽  
Amyloid Polyneuropathy ◽  
Bence Jones Proteinuria
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