The question of trisomy 22 syndrome
β Scribed by R.M. Goodman; M. Bat-Miriam Katznelson; M. Spero; R. Shaki; B. Padeh; N. Sadan
- Book ID
- 118536449
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- English
- Weight
- 167 KB
- Volume
- 79
- Category
- Article
- ISSN
- 1097-6833
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Trisomy 22 was detected in a 32-week-old fetus born to an overweight mother with hypertension. Severe intrauterine growth retardation was associated with phenotypic manifestations of Fryns syndrome: diaphragmatic hernia, facial defects, and nail hypoplasia with short distal fifth phalanges. This is
Mosaic trisomy 22, ascertained in three unrelated patients, was found to be associated with body asymmetry and signs of the Ullrich-Turner syndrome including short stature, ptosis, webbed neck, nevi, cubitus valgus, dysplastic nails, malformed great vessels, and abnormal ovaries. These anomalies in