Results 1 to 10 of about 61 (45)

Acrodermatitis dysmetabolica as a sign of methylmalonic aciduria decompensation [PDF]

Clinical Case Reports (discontinued), 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
exaly   +7 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, Sukina Al Haddad , Reem Medhat Bakraa , Abdulmalik Alqahtani   +3 more
doaj   +4 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, Alessandra Cassio, Valeria Di Natale, Federico Baronio, Rita Ortolano, Andrea Pession, Bianca Maria Piraccini, Iria Neri   +7 more
doaj   +4 more sources

Acrodermatitis dysmetabolica with concomitant acquired acrodermatitis enteropathica in a patient with maple syrup urine disease [PDF]

JAAD Case Reports
Luis E. Santaliz-Ruiz, IV, MD, Angélica C. Marrero-Pérez, MD, Julio Sánchez-Pont, MD, Oscar Nevárez-Pomales, MD   +3 more
exaly   +6 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, Puthita Saengpanit, Ponghatai Damrongphol, Kanya Suphapeetiporn, Sirinuch Chomtho   +4 more
doaj   +3 more sources

Acrodermatitis enteropathica-like eruption [PDF]

JAAD Case Reports, 2022
Farah El Hadadi, MD, Line Mezni, MD, Nadia Ismaili, MD, PhD, Laila Benzekri, MD, PhD, Karima Senouci, MD, PhD   +4 more
doaj   +2 more sources

Acrodermatitis enteropathica in the pediatric population: a literature review of real-world studies [PDF]

Frontiers in Nutrition
Ningning Wang, Wang Ningning, Xu Xuegang   +2 more
exaly   +2 more sources

Acrodermatitis Dysmetabolica: A Masquerade

Indian Journal of Paediatric Dermatology
Abstract 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, Bhumesh Kumar Katakam, Pavani Kusuma, Prashanthi Mogili   +3 more
openaire   +1 more source

Acrodermatitis dysmetabolica with argininosuccinate lyase deficiency

Indian Journal of Dermatology, Venereology and Leprology, 2023
AYDOĞAN, KENAN, SARICAOĞLU, HAYRİYE, ERDÖL, ŞAHİN, Ünlü, Cansu Irmak, Öztürk, FERDİ   +4 more
openaire   +3 more sources

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