Background: actual literature suggests that children of methylmalonic acidemia patients are mostly healthy, but data are only partial, especially regarding long-term outcome. Therefore, our aim was to evaluate the possible long-term neurological effects of fetal exposure to high levels of methylmalonic acid in a child of a renal transplant recipient. Methods: we retrospectively evaluated the clinical and neurological records of a girl whose mother is a kidney transplant recipient affected by methylmalonic acidemia. Subsequently, we compared our results with the ones already published. Results: the girl’s weight and stature were within the normal range in the first years of life but, starting from 4 years of age, she became progressively ove...
Contains fulltext : 69271.pdf (publisher's version ) (Closed access)BACKGROUND: Pl...
Background and objectives: MEGDEL (3-methylglutaconic aciduria with deafness, encephalopathy, and L...
Background: Failure-to-thrive (FTT) has been described in patients with organic acidemias treated wi...
Background: actual literature suggests that children of methylmalonic acidemia patients are mostly h...
Methylmalonic acidemia (MMA) is an inborn error of organic acid metabolism that occurs in infancy wi...
Presently pregnancy is no more exceptional in women with metabolic diseases. However, it still poses...
The renal impairment in children with methylmalonic aciduria has seldom been reported. To improve kn...
OBJECTIVES: MMA is associated with chronic tubulointerstitial nephritis and a progressive decline in...
Methylmalonic acidemia (MMA) is an inborn error of organic acid metabolism. Patients with severe d...
Methylmalonic acidemia (MMA) is an inborn error of organic acid metabolism. Patients with severe dis...
Contains fulltext : 80534.pdf (publisher's version ) (Closed access)Objectives Iso...
Methylmalonic acidemia (aciduria) is an inherited metabolic disturbance from the group of organic ac...
Renal tubular dysfunction and chronic renal failure are well recognised complications of methylmalon...
Methylmalonic acidemia (MMA) is a severe metabolic disorder, particularly with complete deficiency o...
Introduction: MMA is a rare autosomal recessive disorder with the manifestation of recurrent and sev...
Contains fulltext : 69271.pdf (publisher's version ) (Closed access)BACKGROUND: Pl...
Background and objectives: MEGDEL (3-methylglutaconic aciduria with deafness, encephalopathy, and L...
Background: Failure-to-thrive (FTT) has been described in patients with organic acidemias treated wi...
Background: actual literature suggests that children of methylmalonic acidemia patients are mostly h...
Methylmalonic acidemia (MMA) is an inborn error of organic acid metabolism that occurs in infancy wi...
Presently pregnancy is no more exceptional in women with metabolic diseases. However, it still poses...
The renal impairment in children with methylmalonic aciduria has seldom been reported. To improve kn...
OBJECTIVES: MMA is associated with chronic tubulointerstitial nephritis and a progressive decline in...
Methylmalonic acidemia (MMA) is an inborn error of organic acid metabolism. Patients with severe d...
Methylmalonic acidemia (MMA) is an inborn error of organic acid metabolism. Patients with severe dis...
Contains fulltext : 80534.pdf (publisher's version ) (Closed access)Objectives Iso...
Methylmalonic acidemia (aciduria) is an inherited metabolic disturbance from the group of organic ac...
Renal tubular dysfunction and chronic renal failure are well recognised complications of methylmalon...
Methylmalonic acidemia (MMA) is a severe metabolic disorder, particularly with complete deficiency o...
Introduction: MMA is a rare autosomal recessive disorder with the manifestation of recurrent and sev...
Contains fulltext : 69271.pdf (publisher's version ) (Closed access)BACKGROUND: Pl...
Background and objectives: MEGDEL (3-methylglutaconic aciduria with deafness, encephalopathy, and L...
Background: Failure-to-thrive (FTT) has been described in patients with organic acidemias treated wi...