Overview
Fernanda Ludwig-Sperb practices in Rio Grande, Brazil. Ms. Ludwig-Sperb is rated as a Distinguished expert by MediFind in the treatment of Fructose-1,6-Bisphosphatase Deficiency. Her top areas of expertise are Mucolipidosis Type 4, Sialidosis, Mucolipidosis 3, and Biotinidase Deficiency.
Her clinical research consists of co-authoring 45 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 2 articles in the study of Fructose-1,6-Bisphosphatase Deficiency.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Elite
- Mucolipidosis Type 4Ms. Ludwig-Sperb isElite. Learn about Mucolipidosis Type 4.
- Distinguished
- Biotinidase DeficiencyMs. Ludwig-Sperb isDistinguished. Learn about Biotinidase Deficiency.
- Dihydrolipoamide Dehydrogenase DeficiencyMs. Ludwig-Sperb isDistinguished. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Fructose-1,6-Bisphosphatase DeficiencyMs. Ludwig-Sperb isDistinguished. Learn about Fructose-1,6-Bisphosphatase Deficiency.
- Mucolipidosis 3Ms. Ludwig-Sperb isDistinguished. Learn about Mucolipidosis 3.
- Multiple Carboxylase DeficiencyMs. Ludwig-Sperb isDistinguished. Learn about Multiple Carboxylase Deficiency.
- SialidosisMs. Ludwig-Sperb isDistinguished. Learn about Sialidosis.
- Advanced
- Hereditary Fructose IntoleranceMs. Ludwig-Sperb isAdvanced. Learn about Hereditary Fructose Intolerance.
- HomocystinuriaMs. Ludwig-Sperb isAdvanced. Learn about Homocystinuria.
- Inborn Amino Acid Metabolism DisorderMs. Ludwig-Sperb isAdvanced. Learn about Inborn Amino Acid Metabolism Disorder.
- Maple Syrup Urine DiseaseMs. Ludwig-Sperb isAdvanced. Learn about Maple Syrup Urine Disease.
- Von Gierke DiseaseMs. Ludwig-Sperb isAdvanced. Learn about Von Gierke Disease.
- Experienced
- CitrullinemiaMs. Ludwig-Sperb isExperienced. Learn about Citrullinemia.
- Classic GalactosemiaMs. Ludwig-Sperb isExperienced. Learn about Classic Galactosemia.
- DysarthriaMs. Ludwig-Sperb isExperienced. Learn about Dysarthria.
- Early Infantile Epileptic EncephalopathyMs. Ludwig-Sperb isExperienced. Learn about Early Infantile Epileptic Encephalopathy.
- Farber LipogranulomatosisMs. Ludwig-Sperb isExperienced. Learn about Farber Lipogranulomatosis.
- Galactokinase DeficiencyMs. Ludwig-Sperb isExperienced. Learn about Galactokinase Deficiency.