ceroid lipofuscin
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2018 ◽  
pp. bcr-2017-223376 ◽  
Author(s):  
Nassreen Abdullah ◽  
Niall F Davis ◽  
John Quinn ◽  
Ponnusamy Mohan

Hermansky-Pudlak syndrome (HPS) is a rare genetic disorder characterised by oculocutaneous albinism, bleeding diathesis and end-stage renal disease (ESRD), due to interstitial deposition of ceroid lipofuscin. Renal transplantation is potentially a definitive treatment option for patients with ESRD due to HPS. Herein, we describe the case of a 55-year-old male patient with HPS that successfully underwent a living donor kidney transplant. We also emphasise the importance of multidisciplinary input during the preoperative, perioperative and postoperative phases in this high-risk clinical scenario.


2017 ◽  
Vol 51 (3) ◽  
Author(s):  
Mary Anne D. Chiong ◽  
Benilda C. Sanchez-Gan

The neuronal ceroid lipofuscinoses correspond to a group of disorders characterized by neurodegeneration and intracellular buildup of auto-flourescent lipopigment (ceroid lipofuscin). They are classified by age of onset into infantile, late infantile, juvenile and adult forms. Among these, the late infantile type is caused by mutations in tripeptidyl peptidase 1 (TPP1) gene and is characterized by age of onset between 2-4 years, seizures, early progressive cognitive impairment and visual loss. Our patient is a 4-year-old girl who presented at 2 years and 10 months old with seizures followed by ataxia, regression of skills and eventual visual decline. TPP1 enzyme activity was below normal for age. This report aims to increase the awareness of physicians on the cluster of symptoms characteristic of this disorder which will help facilitate early diagnosis and prompt institution of appropriate management.


2017 ◽  
Vol 63 (1) ◽  
pp. 100-114 ◽  
Author(s):  
Douglas E. Brenneman ◽  
David A. Pearce ◽  
Attila Kovacs ◽  
Shawn DeFrees

2017 ◽  
Vol 32 (8) ◽  
pp. 1259-1260 ◽  
Author(s):  
Rossana Terlizzi ◽  
Maria Lucia Valentino ◽  
Anna Bartoletti-Stella ◽  
Marta Columbaro ◽  
Silvia Piras ◽  
...  

2008 ◽  
Vol 1 (2) ◽  
pp. 95-96
Author(s):  
Iris L Tong ◽  
Ghada Bourjeily

Hermansky-Pudlak syndrome (HPS) is a disease characterized by the triad of oculocutaneous albinism, bleeding diathesis and organ failure secondary to lysosomal accumulation of ceroid lipofuscin. We report the case of a pregnant woman with HPS who had a successful vaginal delivery with the administration of desmopressin.


2008 ◽  
Vol 34 (3) ◽  
pp. 282-295 ◽  
Author(s):  
Xinhui Wang ◽  
Yanyang Liao ◽  
Guolin Li ◽  
Dazhong Yin ◽  
Shuli Sheng

Author(s):  
Dazhong Yin ◽  
Ulf Brunk
Keyword(s):  

2000 ◽  
Vol 20 (18) ◽  
pp. 6898-6906 ◽  
Author(s):  
Masato Koike ◽  
Hiroshi Nakanishi ◽  
Paul Saftig ◽  
Junji Ezaki ◽  
Kyoko Isahara ◽  
...  

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