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The infantile-onset form of Pompe disease: an autopsy diagnosis
Otávio César Cruz Dos Santos1, Regina Schultz1
1Department of Pathology - Hospital das Clínicas - Faculty of Medicine - University of São Paulo, São Paulo/SP - Brazil .
Abstract:
Pompe disease (PD) is a rare, inherited autosomal recessive metabolic disorder caused by the deficiency of the lysosomal acid alpha-glucosidase (GAA) enzyme described in 1932 by the Dutch pathologist Joannes Cassianus Pompe. The prevalence of PD ranges from 1:40,000 to 1:300,000 births and depends on geographic and ethnic factors. Clinical manifestations may vary from a rapidly progressive disabling disease with cardiomegaly, hepatomegaly, weakness, generalized hypotonia, and death within the first year of life, to a mild presentation characterized by slowly progressive myopathy predominantly involving the skeletal muscles. The laboratory diagnostic gold standard is represented by the determination of the alpha-glucosidase activity. However, the muscle histology may also yield the diagnosis by evaluating the tissular glycogen accumulation. Until recently, supportive measures constituted the unique available therapy. Currently, the administration of the recombinant GAA is being used with promising results. The authors present the case of a 5-month-old boy, previously diagnosed with hypertrophic cardiomyopathy since the age of 2 months, who presented acute heart failure accompanied by biventricular dilation followed by refractory shock and death. The autopsy findings confirmed the glycogen-accumulation disease.
Insights
Pompe disease, a rare metabolic disorder, results from deficient alpha-glucosidase enzyme activity. This case highlights fatal infantile Pompe disease presenting as heart failure, underscoring the need for early diagnosis.
Area of Science:
- Biochemistry
- Genetics
- Pediatrics
Background:
- Pompe disease is a rare, inherited metabolic disorder caused by acid alpha-glucosidase (GAA) deficiency.
- Prevalence varies globally, with diverse clinical presentations from severe infantile to milder adult forms.
- Diagnosis relies on enzyme activity assays and muscle histology showing glycogen accumulation.
Observation:
- The case involved a 5-month-old infant with hypertrophic cardiomyopathy diagnosed at 2 months.
- The infant presented with acute heart failure, biventricular dilation, and refractory shock.
- Autopsy confirmed glycogen accumulation consistent with Pompe disease.
Findings:
- This case illustrates a fatal presentation of infantile Pompe disease.
- The rapid progression to heart failure and shock in this infant highlights the severe end of the disease spectrum.
- Autopsy findings confirmed glycogen accumulation as the underlying pathology.
Implications:
- Early diagnosis and intervention are crucial for managing Pompe disease, especially in infants.
- Recombinant GAA enzyme replacement therapy offers promising results for patients.
- Understanding the varied clinical spectrum is essential for timely diagnosis and treatment of Pompe disease.
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