Sengers syndrome

From WikiMD's Medical Encyclopedia

Revision as of 15:19, 8 April 2025 by Prab (talk | contribs) (CSV import)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD's medical weight loss NYC, sleep center NYC
Philadelphia medical weight loss and Philadelphia sleep clinics

Sengers syndrome
Synonyms Congenital cataracts hypertrophic cardiomyopathy mitochondrial myopathy
Pronounce
Specialty Medical genetics
Symptoms Congenital cataracts, hypertrophic cardiomyopathy, mitochondrial myopathy, exercise intolerance
Complications N/A
Onset Infancy
Duration Lifelong
Types N/A
Causes Mutations in the AGK gene
Risks
Diagnosis Genetic testing, clinical evaluation
Differential diagnosis Other mitochondrial disorders
Prevention Genetic counseling
Treatment Symptomatic management
Medication
Prognosis Variable, often poor
Frequency Rare
Deaths


Sengers syndrome is a rare genetic disorder characterized by a combination of congenital cataracts, cardiomyopathy, and mitochondrial myopathy. It is inherited in an autosomal recessive manner and is caused by mutations in the AGK gene.

Presentation[edit]

Individuals with Sengers syndrome typically present with congenital cataracts at birth, which can lead to visual impairment if not treated. Cardiomyopathy is another hallmark of the syndrome, often manifesting as hypertrophic cardiomyopathy or dilated cardiomyopathy. Mitochondrial myopathy results in muscle weakness and exercise intolerance. Other features may include growth retardation, lactic acidosis, and hypotonia.

Genetics[edit]

Sengers syndrome is caused by mutations in the AGK gene, which encodes the enzyme acylglycerol kinase. This enzyme is involved in the metabolism of mitochondria, the energy-producing structures within cells. The disorder follows an autosomal recessive inheritance pattern, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected.

Diagnosis[edit]

Diagnosis of Sengers syndrome is based on clinical features, family history, and genetic testing. Molecular genetic testing can confirm the presence of mutations in the AGK gene. Additional diagnostic tests may include echocardiography to assess cardiomyopathy, muscle biopsy to evaluate mitochondrial myopathy, and ophthalmologic examination to detect congenital cataracts.

Management[edit]

There is no cure for Sengers syndrome, and treatment is primarily supportive. Management of congenital cataracts may involve surgical removal to improve vision. Cardiomyopathy is managed with medications and, in severe cases, may require heart transplantation. Physical therapy and occupational therapy can help manage muscle weakness and improve quality of life.

Prognosis[edit]

The prognosis for individuals with Sengers syndrome varies depending on the severity of the symptoms. Early diagnosis and appropriate management can improve outcomes, but the condition can be life-threatening, particularly due to complications related to cardiomyopathy.

See also[edit]

Stub icon
   This article is a genetic disorder stub. You can help WikiMD by expanding it!




Stub icon
   This article is a medical stub. You can help WikiMD by expanding it!



Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes


Ad. Transform your life with W8MD's

GLP-1 weight loss injections special from $29.99 with insurance

Advertise on WikiMD


WikiMD Medical Encyclopedia

Medical Disclaimer: WikiMD is for informational purposes only and is not a substitute for professional medical advice. Content may be inaccurate or outdated and should not be used for diagnosis or treatment. Always consult your healthcare provider for medical decisions. Verify information with trusted sources such as CDC.gov and NIH.gov. By using this site, you agree that WikiMD is not liable for any outcomes related to its content. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.