Bronchial asthma, recurrent croup and bronchiectasis in a child with Crouzon syndrome: clinical observation
Crouzon syndrome (craniofacial dysostosis) is an autosomal dominant disorder, a form of craniosynostosis syndrome; characterized by premature closure of cranial sutures, midfacial hypoplasia, lower mandibular prognathism, marked proptosis and strabismus [1]. The eponymous name of the syndrome comes...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | Russian |
| Published: |
Remedium Group LLC
2014-12-01
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| Series: | Медицинский совет |
| Subjects: | |
| Online Access: | https://www.med-sovet.pro/jour/article/view/589 |
| Summary: | Crouzon syndrome (craniofacial dysostosis) is an autosomal dominant disorder, a form of craniosynostosis syndrome; characterized by premature closure of cranial sutures, midfacial hypoplasia, lower mandibular prognathism, marked proptosis and strabismus [1]. The eponymous name of the syndrome comes from the name of Octave Crouzon, the French neurologist, who first described a craniofacial dysostosis in a mother and her daughter in 1912 [2]. |
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| ISSN: | 2079-701X 2658-5790 |