fa گزارش یک مورد نادر از بیماری متیل مالونیک اسیدمی با هیپرگلیسمی ونوتروپنی وموکورمایکوزیس کارآزمایی بالینی Clinical Trials <p dir="ltr" style="text-align: justify"></p> <div dir="ltr"><p style="text-align: justify"></p> <p style="text-align: justify">Methyl malonic acidemia is an autosomal recessive disease with presentations of mental retardation, recurrent vomiting, ketoacidotic attacks, dehydration, shock, hypoglycemia and hyperamonemia. It will lead to coma and death if unrecognized and untreated. Methyl malonic acidemia may have different skin manifestations. The involvement of blood cells leads to neutropenia, thrombocytopenia and pancytopenia. Most patients have hypoglycemia which in rare cases may be associated with hyperglycemia. The association of mucormycosis, neutropenia and hyperglycemia has been reported in some cases. The case reported in this article carried all three complications together.</p> </div> <p></p><p></p><p></p><p dir="ltr" style="text-align: justify"></p><p dir="ltr" style="text-align: justify"></p><p dir="ltr" style="text-align: justify"></p> Keywords: Methyl malonic acidemia, Mucormycosis, Neutropenia, Hyperglycemia 120 124 http://journal.zums.ac.ir/browse.php?a_code=A-10-4-908&slc_lang=fa&sid=1 Mansour Sadeghzadeh منصور صادق زاده 5200319475328460058857 5200319475328460058857 No Metabolic Disease Research Center, Ayatollah Moussavi Hospital, Zanjan University of Medical Sciences. دانشگاه علوم پزشکی زنجان Parisa Khoshnevisasl پریسا خوشنویس اصل Khoshnevis@zums.ac.ir 5200319475328460058858 5200319475328460058858 Yes Social Determinant of Health Research Center, Ayatollah Moussavi Hospital, Zanjan University of Medical Sciences. دانشگاه علوم پزشکی زنجان