Autofluorescent Ceroid/Lipofuscin

2003 ◽  
pp. 217-228
Author(s):  
Dazhong Yin ◽  
Ulf Brunk
Keyword(s):  
Ceroid Lipofuscin

Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation

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

Ceroid, lipofuscin and the ceroid-lipofuscinoses (Batten Disease)

1993 ◽  
Vol 16 (2) ◽  
pp. 280-283 ◽  
Author(s):  
R. D. Jolly ◽  
R. R. Dalefield ◽  
D. N. Palmer
Keyword(s):  
Batten Disease ◽  
Ceroid Lipofuscin

scholarly journals Neuronal Ceroid-lipofuscinosis in a Cat

1995 ◽  
Vol 32 (5) ◽  
pp. 485-488 ◽  
Author(s):  
R. Bildfell ◽  
C. Matwichuk ◽  
S. Mitchell ◽  
P. Ward
Keyword(s):  
Neuronal Ceroid Lipofuscinosis ◽  
Clinical Signs ◽  
Neuronal Ceroid Lipofuscinoses ◽  
Neurologic Disease ◽  
Ceroid Lipofuscinosis ◽  
Neural Tissues ◽  
Retinal Atrophy ◽  
The Brain ◽  
Reactive Astrocytosis ◽  
Ceroid Lipofuscin

Neuronal ceroid-lipofuscinosis was diagnosed in a young adult domestic short-haired cat euthanatized because of severe progressive neurologic disease. Clinical signs included blindness, seizures, and decreased mentation. An autofluorescent pigment, identified as ceroid-lipofuscin by electron microscopy and staining properties, was found within neurons of the central and peripheral nervous systems. A diffuse reactive astrocytosis accompanied by multifocal microgliosis was visible in all areas of the brain. Retinal atrophy with intraneuronal lipopigment accumulation was also identified. Contrary to the human neuronal ceroid-lipofuscinoses, pigment deposition appeared to be restricted to neural tissues.

scholarly journals Living donor renal transplant in a patient with end-stage renal disease due to Hermansky-Pudlak syndrome

2018 ◽  
pp. bcr-2017-223376 ◽  
Author(s):  
Nassreen Abdullah ◽  
Niall F Davis ◽  
John Quinn ◽  
Ponnusamy Mohan
Keyword(s):  
Renal Disease ◽  
End Stage Renal Disease ◽  
Living Donor ◽  
Genetic Disorder ◽  
Oculocutaneous Albinism ◽  
Definitive Treatment ◽  
Hermansky Pudlak Syndrome ◽  
Stage Renal Disease ◽  
End Stage ◽  
Ceroid Lipofuscin

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.

A Comparative Study of Artificial Ceroid/Lipofuscin from Different Tissue Materials of Rats

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