Mitochondrial Disorders

From WikiGenetics

Contents 1 Name of Condition 2 Definition 3 Description, Signs and Symptoms 4 Inheritance 5 Demographics 6 Diagnosis 7 Treatment and Management 8 Prognosis 9 Resources 10 References

[edit] Name of Condition

[edit] Definition

[edit] Description, Signs and Symptoms

[edit] Inheritance

[edit] Demographics

[edit] Diagnosis

[edit] Treatment and Management

[edit] Prognosis

[edit] Resources

AccessDNA.com - Mitochondrial Conditions: http://www.AccessDNA.com/condition/Mitochondrial_Conditions/252

AccessDNA.com - Mitochondrial Encephalomyopathy, Lactic_acidosis, and_Stroke-like Episodes (MELAS): http://www.AccessDNA.com/condition/Mitochondrial_Encephalomyopathy,_Lactic_acidosis,_and_Stroke-like_Episodes/250

AccessDNA.com - Mitochondrial Trifunctional Protein Deficiency: http://www.AccessDNA.com/condition/Mitochondrial_Trifunctional_Protein_Deficiency/251

AccessDNA.com - Neuropathy, Ataxia and Retinitis Pigmentosa (NARP): http://www.AccessDNA.com/condition/Neuropathy,_Ataxia_and_Retinitis_Pigmentosa/267

AccessDNA.com - Leber Hereditary Optic Neuropathy (LHON): http://www.AccessDNA.com/condition/Leber_Hereditary_Optic_Neuropathy/222]

[edit] References