Severe congenital thrombocytopaenia - First clinical manifestation of Noonan syndrome

BMJ Case Reports

Volumn , Issue , 2012, Pages

  Nunes, Paula ^a   Aguilar, Sara ^b   Prado, Sara Noéme ^c   Palaré, Maria João ^b   Ferrão, Anabela ^b   Morais, Anabela ^b  

^a HOSPITAL DE SÃO FRANCISCO XAVIER   (Portugal)

^b HOSPITAL DE SANTA MARIA   (Portugal)

^c Pediatrics Department   (Portugal)

Author keywords

[No Author keywords available]

Indexed keywords

AORTA VALVE DISEASE; AORTIC VALVE DYSPLASIA; ARTICLE; CASE REPORT; CHROMOSOME ANALYSIS; CLINICAL FEATURE; CRYPTORCHISM; DIFFERENTIAL DIAGNOSIS; DISEASE SEVERITY; FACE DYSMORPHIA; FANCONI ANEMIA; FOLLOW UP; GENE; GENE MUTATION; GENETIC IDENTIFICATION; HEART ATRIUM SEPTUM DEFECT; HEART MURMUR; HUMAN; HYDRAMNIOS; KARYOTYPE 46,XY; MALE; NEONATAL THROMBOCYTOPENIA; NEWBORN; NOONAN SYNDROME; OUTCOME ASSESSMENT; PRIORITY JOURNAL; PTPN11 GENE; RADIUS APLASIA; THROMBOCYTE COUNT; THROMBOCYTE TRANSFUSION; TRANSTHORACIC ECHOCARDIOGRAPHY;

EID: 84860792557     PISSN: None     EISSN: 1757790X     Source Type: Journal    
DOI: 10.1136/bcr.10.2011.4940     Document Type: Article

References (15)

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