Introduction to Mitochondrial Disorders
and Mito Resources
by Susan Agrawal, editor
MitoAction: MitoAction is a group providing support, education, and advocacy for families affected by Mitochondrial Disorders. Of particular interest is the MitoAction Blog, which contains both medical and nonmedical articles similar to those found here at Complex Child, but focused exclusively on Mito.
United Mitochondrial Disease Foundation: UMDF provides medical information, education, and research on Mitochondrial Diseases.
Muscular Dystrophy Association: Mitochondrial Diseases fall under the umbrella of conditions served by MDA. This organization provides a wide variety of supports, including clinics, summer camps, and funding research.
Mitochondria Research Society: Primarily intended for scientists and physicians, this group focuses on research to find a cure for Mitochondrial Diseases.
Parent-2-Parent Mito Support Group: An online community for Mito issues.
The Spectrum of Mitochondrial Disease: An overview of Mito
and Mito Resources
by Susan Agrawal, editor
This month's edition takes a brief look at Mitochondrial Disorders, a collection of genetic diseases that affect the mitochondria
within cells by limiting the amount of energy they can produce. Since
mitochondria are responsible for creating energy within the cell,
thereby supporting organ function and energy throughout the body,
defects in the mitochondria lead to a wide variety of chronic
conditions with variable symptoms and severities.
How many of our readers have heard of MNGIE, Leigh Disease, or Complex I Deficiency? These are just a few of the many disorders considered to be Mitochondrial Diseases, many of which are listed below in Table 1.1 While relatively common (about 1 in 3000-4000 births), and perhaps even more common than thought in milder forms, it is only within the past few years that scientists and doctors have begun to focus more on Mitochondrial Diseases. Awareness of Mitochondrial Disorders remains in its infancy for the public at large, and our hope is that this edition will help to provide more information and awareness about these diseases.
Table 1: Mitochondrial Diseases
Alpers Disease
Barth syndrome
Beta-oxidation Defects
Carnitine-Acyl-Carnitine Deficiency
Carnitine Deficiency
Co-Enzyme Q10 Deficiency
Complex I Deficiency
Complex II Deficiency
Complex III Deficiency
Complex IV Deficiency
Complex V Deficiency
COX Deficiency
CPEO
CPT I Deficiency
CPT II Deficiency
Glutaric Aciduria Type II
KSS
Lactic Acidosis
LCAD
LCHAD
Leigh Disease or Syndrome
LHON
LIC (Lethal Infantile Cardiomyopathy)
Luft Disease
MAD
MCAD
MELAS
MERRF
Mitochondrial Cytopathy
Mitochondrial DNA Depletion
Mitochondrial Encephalopathy
Mitochondrial Myopathy
MNGIE
NARP
Pearson Syndrome
Pyruvate Carboxylase Deficiency
Pyruvate Dehydrogenase Deficiency
Respiratory Chain
SCAD
SCHAD
VLCAD
Because Mitochondrial Diseases vary so much from individual to individual, it is impossible to list out the symptoms, method of diagnosis, treatments, or prognosis for Mitochondrial Diseases. Instead, one must take the approach of Keely Schellenberg in her article, Symptoms of Mito: A Surprisingly Short List, a piece that looks at systems of the body instead of individual symptoms when considering Mito as a diagnosis. Melody Pohla's article, Diagnosing Mitochondrial Disorder: Our Journey through the Genetic Jungle, tackles the difficult area of searching for the specific genetic mutation for her family's Mitochondrial Disorder, providing detailed information on genetics, inheritance, and diagnosis. Finally, Jennifer Peterson's article, Mito Plus: One Family's Experience with Mito, Autism, and Eosinophilic Disease, evaluates how these apparently unrelated conditions may in fact be closely related for her child and many others.
This edition also offers two poignant commentaries from families dealing with Mito. Cristy Balcells' Looking Normal provides a humorous glimpse into day-to-day life for a Mito family. Melody Pohla's The Pregnancy Journal of a Mito Mom takes us through being pregnant with suspected Mito, as well as the early days of her three children, two diagnosed with Mito and one likely to be diagnosed in the future.
Finally, our Specialty Articles and Features sections contain several articles that are helpful to families dealing with Mito as well as many other conditions. An article on Fluid Requirements comes just in time for the summer heat. Two other articles introducing Palliative Care and discussing the Crisis in Pain Control for Children who are Complex, Non-Verbal, or Cognitively Impaired, provide vital information for families confronting difficult issues resulting from life-threatening diseases and chronic pain.
We hope you enjoy this edition!
Mito ResourcesHow many of our readers have heard of MNGIE, Leigh Disease, or Complex I Deficiency? These are just a few of the many disorders considered to be Mitochondrial Diseases, many of which are listed below in Table 1.1 While relatively common (about 1 in 3000-4000 births), and perhaps even more common than thought in milder forms, it is only within the past few years that scientists and doctors have begun to focus more on Mitochondrial Diseases. Awareness of Mitochondrial Disorders remains in its infancy for the public at large, and our hope is that this edition will help to provide more information and awareness about these diseases.
Table 1: Mitochondrial Diseases
Alpers Disease
Barth syndrome
Beta-oxidation Defects
Carnitine-Acyl-Carnitine Deficiency
Carnitine Deficiency
Co-Enzyme Q10 Deficiency
Complex I Deficiency
Complex II Deficiency
Complex III Deficiency
Complex IV Deficiency
Complex V Deficiency
COX Deficiency
CPEO
CPT I Deficiency
CPT II Deficiency
Glutaric Aciduria Type II
KSS
Lactic Acidosis
LCAD
LCHAD
Leigh Disease or Syndrome
LHON
LIC (Lethal Infantile Cardiomyopathy)
Luft Disease
MAD
MCAD
MELAS
MERRF
Mitochondrial Cytopathy
Mitochondrial DNA Depletion
Mitochondrial Encephalopathy
Mitochondrial Myopathy
MNGIE
NARP
Pearson Syndrome
Pyruvate Carboxylase Deficiency
Pyruvate Dehydrogenase Deficiency
Respiratory Chain
SCAD
SCHAD
VLCAD
Because Mitochondrial Diseases vary so much from individual to individual, it is impossible to list out the symptoms, method of diagnosis, treatments, or prognosis for Mitochondrial Diseases. Instead, one must take the approach of Keely Schellenberg in her article, Symptoms of Mito: A Surprisingly Short List, a piece that looks at systems of the body instead of individual symptoms when considering Mito as a diagnosis. Melody Pohla's article, Diagnosing Mitochondrial Disorder: Our Journey through the Genetic Jungle, tackles the difficult area of searching for the specific genetic mutation for her family's Mitochondrial Disorder, providing detailed information on genetics, inheritance, and diagnosis. Finally, Jennifer Peterson's article, Mito Plus: One Family's Experience with Mito, Autism, and Eosinophilic Disease, evaluates how these apparently unrelated conditions may in fact be closely related for her child and many others.
This edition also offers two poignant commentaries from families dealing with Mito. Cristy Balcells' Looking Normal provides a humorous glimpse into day-to-day life for a Mito family. Melody Pohla's The Pregnancy Journal of a Mito Mom takes us through being pregnant with suspected Mito, as well as the early days of her three children, two diagnosed with Mito and one likely to be diagnosed in the future.
Finally, our Specialty Articles and Features sections contain several articles that are helpful to families dealing with Mito as well as many other conditions. An article on Fluid Requirements comes just in time for the summer heat. Two other articles introducing Palliative Care and discussing the Crisis in Pain Control for Children who are Complex, Non-Verbal, or Cognitively Impaired, provide vital information for families confronting difficult issues resulting from life-threatening diseases and chronic pain.
We hope you enjoy this edition!
MitoAction: MitoAction is a group providing support, education, and advocacy for families affected by Mitochondrial Disorders. Of particular interest is the MitoAction Blog, which contains both medical and nonmedical articles similar to those found here at Complex Child, but focused exclusively on Mito.
United Mitochondrial Disease Foundation: UMDF provides medical information, education, and research on Mitochondrial Diseases.
Muscular Dystrophy Association: Mitochondrial Diseases fall under the umbrella of conditions served by MDA. This organization provides a wide variety of supports, including clinics, summer camps, and funding research.
Mitochondria Research Society: Primarily intended for scientists and physicians, this group focuses on research to find a cure for Mitochondrial Diseases.
Parent-2-Parent Mito Support Group: An online community for Mito issues.
The Spectrum of Mitochondrial Disease: An overview of Mito
1List taken from UMDF at http://www.umdf.org/site/c.dnJEKLNqFoG/b.3042173