Carbimazole Embryopathy and Choanal Atresia
نویسندگان
چکیده
منابع مشابه
Carbimazole Embryopathy and Choanal Atresia
Congenital choanal atresia (CCA), especially the bilateral form, is a rare neonatal emergency. Its incidence is usually quoted as 1 in 5000 8000 live-births. [1] However, a recent epidemiological study involving more than 2.2 million deliveries suggests that CCA is extremely rare with a calculated incidence of 3 to 9 per 100,000 livebirths. [2] Athena is fascinated by CCA not only due to its ra...
متن کاملChoanal atresia.
Choanal atresia is caused by failure of resorption of the bucco-pharyngeal membrane during embryonic development. The atresia can be membranous or bony in nature, but is usually mixed in most cases. When the atresia is bilateral, newborns can have severe airway distress and cyanosis is alleviated by crying. Bilateral choanal atresia is managed with an oropharyngeal airway. Flexible nasal endosc...
متن کاملCongenital choanal atresia.
Congenital choanal atresia (CCA) is the developmental failure of the nasal cavity to communicate with the nasopharynx. Bilateral choanal atresia is potentially life threatening in newborns. Most of these cases present early in life with cyclical phases of respiratory distress and apnoea, which gets relieved by crying. In fewer cases it goes undiagnosed to present in adult life with rhinorrhoea ...
متن کاملCongenital bilateral choanal atresia.
Congenital choanal atresia (CCA) is the developmental failure of the nasal cavity to communicate with nasopharynx. Surgical repair is recommended in the first weeks of life in bilateral cases because this is a life-threatening situation in newborns. This is a case report of a full-term, healthy newborn baby presenting with intermittent attacks of cyanosis and respiratory distress soon after bir...
متن کاملCongenital choanal atresia.
We have treated a total of 15 patients (11 girls, 4 boys) for choanal atresia in the University Department of Otorhinolaryngology during a period of 15 years from 1963-1976. No other cases occurred in their families. One patients is mentally retarded, whereas none of the others have had other congenital defects. Five patients (4 girls, 1 boy) had bilateral choanal atresia. In all 5 cases, the b...
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ژورنال
عنوان ژورنال: Journal of Neonatal Surgery
سال: 2014
ISSN: 2226-0439
DOI: 10.47338/jns.v3.69