Congenital nasal pyriform aperture stenosis: Diagnosis and management of 20 cases

Annals of Otology, Rhinology and Laryngology

Volumn 110, Issue 1, 2001, Pages 70-75

  Van den Abbeele, Thierry ^a   Triglia, Jean Michel ^b   François, Martine ^a   Narcy, Philippe ^a  

^a HÔPITAL ROBERT DEBRÉ   (France)

^b TIMONE HOSPITAL   (France)

Author keywords

Infant; Nasal obstruction; Neonate; Pyriform aperture stenosis

Indexed keywords

GROWTH HORMONE; VASOPRESSIN;

ACROCEPHALOSYNDACTYLY; ARTICLE; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; FEMALE; FOLLOW UP; HORMONE DEFICIENCY; HUMAN; HYPOPHYSIS DISEASE; INFANT; MALE; NEWBORN; NOSE MALFORMATION; NOSE OBSTRUCTION; PHYSICAL EXAMINATION; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; MALE; NASAL CAVITY; NASAL OBSTRUCTION;

EID: 0035141846     PISSN: 00034894     EISSN: None     Source Type: Journal    
DOI: 10.1177/000348940111000113     Document Type: Article

References (8)

1. Congenital nasal pyriform aperture stenosis
2. Congenital nasal pyriform aperture stenosis. Isolated abnormality vs developmental field defect
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5. Nasal pyriform aperture stenosis and the holoprosencephaly spectrum
6. The face predicts the brain: Diagnostic significance of median facial anomalies for holoprosencephaly (arhinencephaly)
7. Solitary maxillary central incisor and short stature
8. Perspectives on holoprosencephaly: Part I. Epidemiology, genetics and syndromology