Results 1 to 10 of about 30 (26)

Acrodermatitis dysmetabolica as a sign of methylmalonic aciduria decompensation

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   +3 more sources

Skin Lesions Associated with Nutritional Management of Maple Syrup Urine Disease

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   +2 more sources

Acrodermatitis dysmetabolica secondary to isoleucine deficiency in infant with maple syrup urine disease

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   +1 more source

A Case of Acrodermatitis Dysmetabolica in a Child Affected by Citrullinemia Type I: When Early Diagnosis and Timely Treatment Are Not Enough

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   +1 more source

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

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   +3 more sources

Pathophysiology of propionic and methylmalonic acidemias. Part 1: Complications

Journal of Inherited Metabolic Disease, Volume 42, Issue 5, Page 730-744, September 2019., 2019
Abstract Over the last decades, advances in clinical care for patients suffering from propionic acidemia (PA) and isolated methylmalonic acidemia (MMA) have resulted in improved survival. These advances were possible thanks to new pathophysiological insights.
Hanneke A. Haijes, Judith J. M. Jans, Simone Y. Tas, Nanda M. Verhoeven‐Duif, Peter M. van Hasselt   +4 more
wiley   +1 more source

Acrodermatitis Dysmetabolica as a Cutaneous Manifestation of Isoleucine Deficiency in Maple Syrup Urine Disease: A Systematic Review of Reported Cases

Health Science Reports
Background and Aim Maple Syrup Urine Disease (MSUD) is a metabolic disorder affecting branched‐chain amino acid metabolism. While neurological symptoms are well‐characterized, cutaneous manifestations such as acrodermatitis dysmetabolica (AD) caused by ...
Bahareh Abtahi‐naeini, Motahar Heidari‐Beni, Noushin Rostampour, Naeimeh Davoudi, Sarah Seyedyousefi   +4 more
doaj   +1 more source

Acrodermatitis enteropathica-like eruption

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   +1 more source

Acrodermatitis enteropathica and an overview of zinc metabolism

Journal of the American Academy of Dermatology, 2007
Emanual Maverakis, Maxwell Fung, Peter J Lynch   +2 more
exaly  

<p>Acrodermatitis continua of Hallopeau: clinical perspectives</p>

Psoriasis: Targets and Therapy, 2019
Quinn Thibodeaux, Wilson Liao, Tina Bhutani   +2 more
exaly