Congenital erythropoietic porphyria: Prenatal diagnosis and autopsy findings in two sibling fetuses

Pediatric and Developmental Pathology

Volumn 4, Issue 2, 2001, Pages 180-184

  Daikha Dahmane F ^a   Dommergues, M ^b   Narcy, F ^c   Gubler, M C ^b   Dumez, Y ^b   Gauthier, E ^d   Nordmann, Y ^e   Nessmann, C ^a   Terrasse, G ^c   Muller, F ^f  

^a HÔPITAL ROBERT DEBRÉ   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c Faculté de Médecine Cochin Port Royal ^*  (France)

^d AMERICAN HOSPITAL OF PARIS   (France)

^e HÔPITAL LOUIS MOURIER   (France)

^f UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

Congenital erythropoietic porphyria; Fetuses sibs; Hydrops fetalis; Prenatal diagnosis

Indexed keywords

ARTICLE; AUTOPSY; CONGENITAL ERYTHROPOIETIC PORPHYRIA; FETUS; FETUS HYDROPS; GENE MUTATION; HUMAN; HUMAN TISSUE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ADULT; AMNIOTIC FLUID; AUTOPSY; DNA; FATAL OUTCOME; FEMALE; FLUORESCENCE; GESTATIONAL AGE; HUMANS; HYDROPS FETALIS; MUTATION; NUCLEAR FAMILY; PIGMENTATION; PORPHYRIA, ERYTHROPOIETIC; PREGNANCY; ULTRASONOGRAPHY, PRENATAL; UROPORPHYRINOGENS;

EID: 0035126047     PISSN: 10935266     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100240010143     Document Type: Article

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