Acrodermatitis dysmetabolica as a sign of methylmalonic aciduria decompensation [PDF]
Clinical Case Reports, 2018 Key Clinical Message Methylmalonic aciduria children must follow an adequate diet with low protein intake and should be regularly monitored to prevent complications.
Joana Rosa +5 more
doaj +7 more sources
A Case of Acrodermatitis Dysmetabolica in a Child Affected by Citrullinemia Type I: When Early Diagnosis and Timely Treatment Are Not Enough [PDF]
Children, 2023 An infant with a prenatal diagnosis of citrullinemia, who started standard treatment at birth (L-arginine; sodium benzoate and a personalized diet characterized by a low protein intake and supplementation of essential nutrients and amino acids ...
Laura Bruni +7 more
doaj +6 more sources
Acrodermatitis dysmetabolica with concomitant acquired acrodermatitis enteropathica in a patient with maple syrup urine disease [PDF]
JAAD Case ReportsLuis E. Santaliz-Ruiz, IV, MD +3 more
doaj +6 more sources
Acrodermatitis dysmetabolica secondary to isoleucine deficiency in infant with maple syrup urine disease [PDF]
Dermatology Reports, 2023 Acrodermatitis dysmetabolica (AD) describes eruptions characterized by the clinical triad of acral dermatitis, diarrhea, and alopecia. AD can be caused by various metabolic disorders one of which is maple syrup urine disease (MSUD). We present a 2-month-
Fares A. Alkhayal +3 more
doaj +4 more sources
Skin Lesions Associated with Nutritional Management of Maple Syrup Urine Disease [PDF]
Case Reports in Dermatological Medicine, 2017 Introduction. Maple syrup urine disease (MSUD) is an inborn error of branched chain amino acids (BCAAs) metabolism. We report an infant with MSUD who developed 2 episodes of cutaneous lesions as a result of isoleucine deficiency and zinc deficiency ...
Jaraspong Uaariyapanichkul +4 more
doaj +3 more sources
Acrodermatitis enteropathica-like eruption [PDF]
JAAD Case Reports, 2022 Farah El Hadadi, MD +4 more
doaj +2 more sources
Acrodermatitis dysmetabolica with argininosuccinate lyase deficiency
Indian Journal of Dermatology, Venereology and Leprology, 2023 Kenan Aydoḡan, Şahin Erdol
exaly +4 more sources
Acrodermatitis Dysmetabolica: A Masquerade
Indian Journal of Paediatric DermatologyAbstract Maple syrup urine disease (MSUD) is a rare autosomal-recessive inborn error of branched-chain amino acid (BCAA) metabolism. It is caused by enzymatic defect in the metabolic pathway of branched chain amino acids (leucine, isoleucine, valine) which leads to accumulation of BCAAs and corresponding keto acids in plasma, urine, and ...
Tulasi Jarang +3 more
openaire +1 more source
Clinical and biochemical footprints of inherited metabolic diseases. VI. Metabolic dermatoses. [PDF]
Mol Genet Metab, 2021 Ferreira CR, Martinelli D, Blau N.
europepmc +1 more source
Skin Conditions and Movement Disorders: Hiding in Plain Sight. [PDF]
Mov Disord Clin Pract, 2022 Kulcsarova K +3 more
europepmc +1 more source