Intracerebral mass bleeding in a term neonate: Manifestation of hereditary protein s deficiency with a new mutation in the PROS1 gene

Neonatology

Volumn 98, Issue 4, 2010, Pages 337-340

  Fischer, Doris ^a   Porto, Luciana ^a   Stoll, Hildegard ^b   Geisen, Christof ^c   Schloesser, Rolf L ^a  

^a UNIVERSITY HOSPITAL FRANKFURT   (Germany)

^b Divisions of Haemostaseology ^*  (Germany)

^c GOETHE UNIVERSITY   (Germany)

Author keywords

Coagulation; Coagulopathy; Congenital prothrombotic disorder; Gene mutation; Intracerebral hemorrhage; Protein S deficiency

Indexed keywords

FRESH FROZEN PLASMA; HEPARIN; PHENOBARBITAL; PROTEIN S; SODIUM CHLORIDE; VITAMIN K GROUP;

ABDOMINAL AORTA; ANEMIA; AORTA THROMBOSIS; ARTICLE; ARTIFICIAL VENTILATION; BLOOD SAMPLING; BRAIN HEMORRHAGE; BRAIN HERNIA; CASE REPORT; CORNEA REFLEX; DEATH; DNA ISOLATION; DOPPLER FLOWMETRY; ENDOTRACHEAL INTUBATION; ERYTHROCYTE CONCENTRATE; FLUID RESUSCITATION; GENE MUTATION; GENETIC ANALYSIS; HEAD CIRCUMFERENCE; HEMORRHAGIC SHOCK; HUMAN; ILIAC ARTERY OBSTRUCTION; KIDNEY ARTERY STENOSIS; LEUKOCYTE; MALE; MUSCLE HYPOTONIA; NEUROSURGERY; NEWBORN; NEWBORN SCREENING; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEIC ACID SEQUENCE BASED AMPLIFICATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN S DEFICIENCY; SEIZURE; SEQUENCE ANALYSIS; SUBARACHNOID HEMORRHAGE; THROMBOPHILIA; ULTRASOUND;

BLOOD PROTEINS; CLINICAL CHEMISTRY TESTS; HUMANS; INFANT, NEWBORN; INTRACRANIAL HEMORRHAGES; MAGNETIC RESONANCE IMAGING; MALE; POINT MUTATION; PROTEIN S DEFICIENCY; REFERENCE VALUES;

EID: 77952298178     PISSN: 16617800     EISSN: 16617819     Source Type: Journal    
DOI: 10.1159/000298282     Document Type: Article

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