New PRSS1 and common CFTR mutations in a child with acute recurrent pancreatitis, could be considered an "Hereditary" form of pancreatitis?

BMC Gastroenterology

Volumn 10, Issue , 2010, Pages

  Corleto, Vito D ^a,c   Gambardella, Stefano ^b,e   Gullotta, Francesca ^b   D'Apice, Maria R ^b   Piciucchi, Matteo ^a   Galli, Elena ^c   Lucidi, Vincenzina ^d   Novelli, Giuseppe ^b,e   Fave, Gianfranco D ^a  

^a SAPIENZA UNIVERSITY OF ROME   (Italy)

^b UNIVERSITY OF ROME TOR VERGATA   (Italy)

^c FATEBENEFRATELLI HOSPITAL   (Italy)

^d BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^e Fondazione Livio Patrizi   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AMYLASE; APROTININ; C REACTIVE PROTEIN; CALCIUM; CHYMOTRYPSIN; CHYMOTRYPSIN C; GLUCOSE; INFUSION FLUID; PANCREAS ENZYME; PROTEIN PRSS1; PROTEIN SPINK 1; PROTON PUMP INHIBITOR; SECRETIN; SERINE PROTEASE INHIBITOR OF KAZAL TYPE 1; TRANSMEMBRANE CONDUCTANCE REGULATOR; TRIACYLGLYCEROL; TRIACYLGLYCEROL LIPASE; TRYPSINOGEN; UNCLASSIFIED DRUG; CFTR PROTEIN, HUMAN; PRSS1 PROTEIN, HUMAN; TRYPSIN;

ABDOMINAL DISTENSION; ACUTE ABDOMEN; ACUTE PANCREATITIS; ACUTE RECURRENT PANCREATITIS; AMYLASE BLOOD LEVEL; ANTHROPOMETRY; APPENDECTOMY; ARTICLE; BACK; BODY WEIGHT; CASE REPORT; CHILD; CLINICAL OBSERVATION; COMPARATIVE GENOMIC HYBRIDIZATION; ECHOGRAPHY; ENZYME THERAPY; EPIGASTRIC PAIN; ERYTHROCYTE SEDIMENTATION RATE; EXON; FAMILY HISTORY; FATHER; FEVER; GALLBLADDER; GENE DELETION; GENE INSERTION; GENE MUTATION; GENE REARRANGEMENT; GENETIC ANALYSIS; HETEROZYGOSITY; HOSPITALIZATION; HUMAN; LEUKOCYTE COUNT; LIQUID LIGHT MEAL; LOW FAT DIET; MALE; MEAL; MOTHER; NAUSEA; NEUTROPHIL COUNT; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEIC ACID BASE SUBSTITUTION; POINT MUTATION; PRESCHOOL CHILD; PROTEIN BLOOD LEVEL; RADICULOPATHY; SEQUENCE ANALYSIS; SYMPTOM; TRIACYLGLYCEROL LIPASE BLOOD LEVEL; ACUTE HEMORRHAGIC PANCREATITIS; DIFFERENTIAL DIAGNOSIS; FOLLOW UP; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; METABOLISM; MUTATION; RECURRENT DISEASE;

CHILD; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; DIAGNOSIS, DIFFERENTIAL; EXONS; FOLLOW-UP STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MALE; MUTATION; PANCREATITIS, ACUTE NECROTIZING; RECURRENCE; TRYPSIN;

EID: 77957921193     PISSN: None     EISSN: 1471230X     Source Type: Journal    
DOI: 10.1186/1471-230X-10-119     Document Type: Article

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