A new contribution to the study of 22 trisomy

✍ Scribed by P�rez-Castillo, Amalia ;Abrisqueta, J. A. ;Martin-Lucas, Maria A. ;Goday, Clara ;Mazo, J. ;Aller, V.

• Publisher: Springer-Verlag
• Year: 1975
• Weight: 309 KB
• Volume: 30
• Category: Article
• ISSN: 0018-7348
• DOI: 10.1007/bf00279192

✦ Synopsis

The case of a 2 1/2-month-old male child with intrauterine distrophy features and multiple congenital malformations is presented. Cytogenetic studies of the child and his parents, completed with Q- and G-banding techniques led us to conclude that it is a case of 22 trisomy inherited from his mother.