TY  - GEN
AU  - Cammarata-Scalisi,Francisco
AU  - López-Gallardo,Ester
AU  - Emperador,Sonia
AU  - Ruiz-Pesini,Eduardo
AU  - Da Silva,Gloria
AU  - Camacho,Nolis
AU  - Montoya,Julio
TI  - [Pearson syndrome. Case report]
SN  - 0535-5133
PY  - 2011///1206
KW  - Acyl-CoA Dehydrogenase, Long-Chain
KW  - deficiency
KW  - Anemia, Sideroblastic
KW  - blood
KW  - Congenital Bone Marrow Failure Syndromes
KW  - DNA, Mitochondrial
KW  - genetics
KW  - Diarrhea, Infantile
KW  - etiology
KW  - Exocrine Pancreatic Insufficiency
KW  - Fatal Outcome
KW  - Female
KW  - Humans
KW  - Hypokalemia
KW  - Infant
KW  - Lipid Metabolism, Inborn Errors
KW  - Mitochondrial Diseases
KW  - Muscular Diseases
KW  - Phenotype
KW  - Referral and Consultation
KW  - Sequence Analysis, DNA
KW  - Sequence Deletion
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
ER  -