Central cyanosis and thickening in a thoracic X-ray of an infant;Zentrale zyanose und verdichtungen im thoraxröntgenbild bei einem säugling

Monatsschrift fur Kinderheilkunde

Volumn 155, Issue 9, 2007, Pages 789-792

  Wirbelauer, J ^a   Thomas, W ^a   Darge, K ^a   Singer, D ^a  

^a UNIVERSITY OF WÜRZBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTIC AGENT; ANTIVIRUS AGENT;

ANAMNESIS; ARTERIOVENOUS MALFORMATION; ARTICLE; ARTIFICIAL VENTILATION; BIRTH; BREATHING; DIFFERENTIAL DIAGNOSIS; HEART; HUMAN; LIFE; LUNG; LUNG MALFORMATION; OUTPATIENT DEPARTMENT; PEDIATRICIAN; PNEUMONIA; PREGNANCY; PROGNOSIS; RENDU OSLER WEBER DISEASE; THORAX RADIOGRAPHY;

EID: 34648828859     PISSN: 00269298     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00112-007-1578-6     Document Type: Article

References (5)

1. Berg JN, Guttmacher AE, Archuk DA et al. (1996) Clinical heterogenity in hereditary hemorrhagic teleangiectasia: are pulmonary arteriovenous malformations more common in families linked to endoglin? J Med Genet 33: 256-257
2. Geisthoff UW, Schneider G, Fischinger J et al. (2002) Hereditäre hämorrhagische Teleangiektasie (Morbus Osler). Eine interdisziplinäre Herausforderung. HNO 50: 114-128
3. Heling KS, Tennstedt C, Goldner B et al. (2002) Prenatal diagnosis of intrapulmonary arteriovenous malformation: sonographic and pathomorphological findings. Ultrasound Obstet Gynecol 19: 514-517
4. Saluja S, Henderson KJ, White RI Jr (2000) Embolotherapy in the bronchial and pulmonary circulations. Radiol Clin North Am 38: 425-448
5. Shovlin CL, Guttmacher AE, Buscarini E et al. (2000) Diagnostic criteria for hereditary hemorrhagic teleangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet 91: 66-67