Apert syndrome with partial post-axial polydactyly and unilateral choanal atresia.
نویسندگان
چکیده
The amount of toxin produced and the diarrhea caused by 0 139 serotype are very similar to that caused by V. cholerae 01. This new serotype is sensitive to tetracycline, ampicillin and chloramphenicol, but is resistant to co-trimoxazole (98%), and furazolidine (86%), the latter two agents often used to treat cholrea(2,5). In India even in children, tetracycline for three days or single dose of doxycycline should now be preferred(4).
منابع مشابه
آترزی کوآن دو طرفه در یک نوزاد: گزارش موردی
ABSTRACT Choanal atresia is the most common congenital anomally of the nose and has a frequency of aproximately 1/7000 live births. It consists of a unilateral or bilateral bony (29%) or bony-membranous(71%) wall. Nearly 50% of affected infants have other congenital anomalies or CHARGE syndrome that include: coloboma, heart disease, choanal atresia, growth and development retardation, ...
متن کاملآترزی کوآن: تجربه 13 ساله و بررسی متون: گزارش کوتاه
Choanal atresia was first described by Roeder in 1755.1 Choanal atresia is the narrowing or obstruction of the posterior nasal fossa. This anomaly could be congenital or acquired. Most patients are female.2 Choanal atresia might be isolated or associated with other anomalies like CHARGE syndrome and 20-50% of congenital cases have this company.3 Choanal atresia could be unilateral or bilateral ...
متن کاملUnilateral choanal atresia in one monozygotic twin: a case report.
Unilateral atresia is an extremely uncommon congenital disorder in monozygotic twins. We present the first case in the literature of premature, monozygotic twins with no other congenital genetic defects other than only one twin with unilateral choanal atresia on the right side, being the other sibling completely normal. Diagnostic examinations performed to both twins consisted of nasal endoscop...
متن کاملReader Digest Digested by Dr . Tarek Kandil , MD . Consultant , students Hospital , Cairo University 1 . Management of the Airway in Apert Syndrome
Management of the airway in Apert syndrome is complex and multidisciplinary. This rare syndrome, occurring in up to approximately 1 in 65,000 live births, results in airway compromise at various anatomic levels, in addition to abnormal central respiratory drive. Obstructive apneas arise because of decreased airway caliber, which may occur in the form of congenital bony nasal stenosis, choanal a...
متن کاملFamilial Pallister-Hall syndrome.
In their report of sibs with the Pallister-Hall syndrome, Thomas et al' make the points that choanal atresia may be a feature of this condition and that it may be caused by a dominant gene. We have recently encountered an infant in whom the findings lend support to both of these suggestions. Our patient, a female, was the first child born to a healthy 31 year old female and her healthy and unre...
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عنوان ژورنال:
- Indian pediatrics
دوره 31 7 شماره
صفحات -
تاریخ انتشار 1994