SummaryDermatoglyphic examinations were undertaken on the dermal surfaces of two fetuses at the 20th and 22nd week, respectively, from the onset of the last menstrual periods. The fetuses were diagnosed as cases of trisomy 21 by amniocentesis, and abortions were induced.Although the dermatoglyphics of the fetus have been studied by some workers (Miller, 1968;Okajima, 1975), dermatoglyphic examinations have not been widely applied in fetuses with chromosomal anomalies. In a comprehensive study on spontaneous abortuses and stillbirths, Poland and Lowry (1974) observed dermatoglyphic features typical of some trisomies in three stillborn infants in which karyotyping was not successful. However, they recognized that dermatoglyphic analysis was difficult in many cases due to maceration of the skin. Recently, Suzumori (1980) reported his dermatoglyphic findings in five fetuses with different chromosomal aberrations karyotyped by amniocentesis.The present report describes the dermatoglyphic data obtained in two fetuses in which karyotypes were determined as trisomy 21 by amniocentesis.
MATERIALS AND METHODSThe pregnancies were artificially terminated due to the results of karyotyping by amniocentesis at the 137th day from the onset of the last menstrual period in Case 1 and at the 152nd day in Case 2. The karyotypes of both fetuses were reaffirmed after abortion by the culture of skin fibroblasts. The fetuses were fixed with 10~ formalin after autopsy, and then the hands and feet were delivered to us for dermatoglyphic examination.