And Pallidal Degeneration Retinitis Pigmentosa Acanthocytosis Hypoprebetalipoproteinemia

Also Known As:

Networked: 5 relevant articles (0 outcomes, 2 trials/studies)

Disease Context: Research Results

Related Diseases

1.	And Pallidal Degeneration Retinitis Pigmentosa Acanthocytosis Hypoprebetalipoproteinemia
2.	Giant Axonal Neuropathy
3.	Neuroaxonal Dystrophies (Neuroaxonal Dystrophy, Late Infantile)
4.	Progressive Supranuclear Palsy (Steele Richardson Olszewski Syndrome)
5.	Parkinson Disease (Parkinson's Disease)

Experts

1.	Houlden, H: 2 articles (10/2006 - 11/2003)
2.	Matarin, M M: 1 article (10/2006)
3.	Singleton, A B: 1 article (10/2006)
4.	Cleland, P G: 1 article (11/2003)
5.	Farrer, M: 1 article (11/2003)
6.	Hardy, J: 1 article (11/2003)
7.	Lincoln, S: 1 article (11/2003)
8.	Orrell, R W: 1 article (11/2003)
9.	Ching, K H L: 1 article (06/2002)
10.	Gitschier, J: 1 article (06/2002)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to And Pallidal Degeneration Retinitis Pigmentosa Acanthocytosis Hypoprebetalipoproteinemia:

1.	LipidsIBA 03/01/1995 - "We also report two patients with clinical and radiologic features similar to those of the patient with HARP syndrome but who had normal lipid studies. " 09/01/1996 - "This phenotype closely resembled the so-called HARP syndrome (hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa and pallidal degeneration), but extensive serum lipid study failed to demonstrate any lipoprotein abnormality. "
2.	Lipoproteins (Lipoprotein)IBA 09/01/1996 - "This phenotype closely resembled the so-called HARP syndrome (hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa and pallidal degeneration), but extensive serum lipid study failed to demonstrate any lipoprotein abnormality. "
3.	pleiotrophin (HARP)IBA 11/25/2003 - "The authors describe a patient with hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration (HARP) who has two compound heterozygote mutations of the PANK2 gene. " 06/11/2002 - "HARP (hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration) is a rare syndrome with many clinical similarities to pantothenate kinase-associated neurodegeneration (PKAN, formerly Hallervorden-Spatz syndrome). "
4.	NAD (NADH)IBA 10/23/2006 - "This included cases with neurodegeneration and brain iron accumulation, corticobasal degeneartion, progressive supranuclear palsy (PSP), Parkinson's disease (PD), multiple system atropy, giant axonal neuropathy (GAN), neuroaxonal dystrophy (NAD), Guam dementia and HARP syndrome (pallido-pyramidal syndrome and hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa and pallidal degeneration). "
5.	IronIBA 10/23/2006 - "This included cases with neurodegeneration and brain iron accumulation, corticobasal degeneartion, progressive supranuclear palsy (PSP), Parkinson's disease (PD), multiple system atropy, giant axonal neuropathy (GAN), neuroaxonal dystrophy (NAD), Guam dementia and HARP syndrome (pallido-pyramidal syndrome and hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa and pallidal degeneration). "