We report on the third confirmed case of trisomy 22 in a liveborn infant. High-resolution banding studies ruled out translocations such as the relatively common t(11;22). The infant shared many manifestations with other reported cases of trisomy 22 (e.g., growth deficiency, microcephaly, micrognathi
โฆ LIBER โฆ
Trisomy 22 with congenital diaphragmatic hernia and absence of corpus callosum in a liveborn premature infant
โ Scribed by Kim, Eun H. ;Cohen, Ronald S. ;Ramachandran, Pramela ;Mineta, Albert K. ;Babu, V. Ramesh
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 219 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0148-7299
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An infant with congenital diaphragmatic hernia was delivered by vacuum extraction, with a resultant subgaleal hemorrhage that excluded him from ECMO. The literature regarding vacuum-assisted delivery and birth trauma is reviewed in the context of congenital anomalies that may require ECMO support, a