نتایج جستجو برای: methylmalonic acidemia disorder

تعداد نتایج: 598789  

Journal: :Archives of neurology 2012
Anjail Z Sharrief Joel Raffel David S Zee

OBJECTIVE To describe a case of vitamin B(12) deficiency with classic and rare clinical features and novel radiographic features. DESIGN Case report. SETTING Johns Hopkins Hospital neurology service. PATIENT Middle-aged man with neuropathy, myelopathy,impaired cognition, and extrapyramidal signs. RESULTS The patient had neurologic and hematologic signs of vitamin B(12) deficiency, with ...

Journal: :Journal of the Chinese Medical Association : JCMA 2009
Chuan-Hong Kao Mei-Ying Liu Tze-Tze Liu Kwang-Jen Hsiao Kang-Hsiang Cheng Cheng-Hung Huang Hsiang-Yu Lin Dau-Ming Niu

BACKGROUND Information regarding growth hormone (GH) therapy in neonatal patients with methylmalonic academia (MMA) is lacking. We present our experience with GH therapy in neonatal patients with MMA. METHODS Four neonatal patients with mut 0 type MMA were identified through newborn screening for elevated propionylcarnitine (C3) levels. GH therapy (0.6 IU/kg/week, subcutaneously) was prescrib...

2012
Heidi L. Peters James J. Pitt Leonie R. Wood Natasha J. Hamilton Joseph P. Sarsero Nicole E. Buck

Methylmalonic aciduria (MMA) is a disorder of organic acid metabolism resulting from a functional defect of methylmalonyl-CoA mutase (MCM). MMA is associated with significant morbidity and mortality, thus therapies are necessary to help improve quality of life and prevent renal and neurological complications. Transgenic mice carrying an intact human MCM locus have been produced. Four separate t...

We encountered a patient with methylmalonic aciduria associated with skin lesions resembling acrodermatitis enteropathica. This child was being fed with a low-protein diet when the skin disorder developed. A deficiency in plasma levels isoleucine, was confirmed. Supplementation of a high-caloric, protein-rich diet led to a prompt improvement of skin lesions. We assume that in our patient the sk...

Journal: :Human gene therapy 2014
Edward S Y Wong Chantelle McIntyre Heidi L Peters Enzo Ranieri Donald S Anson Janice M Fletcher

Methylmalonic aciduria is a rare disorder of organic acid metabolism with limited therapeutic options, resulting in high morbidity and mortality. Positive results from combined liver/kidney transplantation suggest, however, that metabolic sink therapy may be efficacious. Gene therapy offers a more accessible approach for the treatment of methylmalonic aciduria than organ transplantation. Accord...

Journal: :The American journal of clinical nutrition 2011
Natalie S Hauser Irini Manoli Jennifer C Graf Jennifer Sloan Charles P Venditti

BACKGROUND Isolated methylmalonic acidemia (MMA) is managed by dietary protein restriction and medical food supplementation. Resting energy expenditure (REE) can be depressed in affected individuals for undefined reasons. OBJECTIVE The objective was to document the spectrum of nutritional approaches used to treat patients with MMA, measure REE, and analyze the dependence of REE on body compos...

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