No abstract available.
Trisomy*

No abstract available.
Trisomy*

No abstract available.
Trisomy*

No abstract available.
Trisomy*

No abstract available.
Mosaicism* ; Trisomy*

There are certain congenital malformations, namely, 13-15 trisomy, Lowe's syndrome, Miller's syndrome, Thalidomide-Phacomella, and Gregg's syndrome which were recently understood in causes and pathogenesis. Characteristic ocular lesions of these malformations are presented briefly from the aspects of ophthalmic pathology.
Pathology ; Trisomy

No abstract available.
Trisomy* ; Ultrasonography*

No abstract available.
Leukemia, Eosinophilic, Acute* ; Trisomy*

Since Yunis and Sanchez described in 1974, distal 10q partial trisomy has been recognised as a chromosomal anomaly, which has typical features, psychomotor delays, distinctive dysmorphic appearance and growth retardation. Also, it is associated with cardiac, renal and ocular anomalies. Most of them result from an unbalanced tanslocation or a deletion but, pure duplications are very rare. We report a 19-month-old boy with typical clinical features of distal 10q partial trisomy with a pure duplicatin of 10q.
Humans ; Infant ; Male ; Trisomy*

Cyclopia is rare congenital craniofacial anomaly, in which the eyes are fused together and located in a single orbit. It is consistently associated with severe holoprosencephaly, which is the failure of cleavage of the prosencephalon with a deficit in the midline facial development. chromosomal study revealed 47, X( ), +13 (Patau syndrome).
Holoprosencephaly ; Orbit ; Prosencephalon ; Trisomy*