Volume 43, Issue 3 pp. 602-605
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Neu-Laxova syndrome: Prenatal ultrasonographic diagnosis, clinical and pathological studies, and new manifestations

Israel Shapiro

Israel Shapiro

Department of Obsterics and Gynecology, Bnai-Zion Medical Center, Technion-Faculty of Medicine, Haifa, Israel

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Dr. Zvi Borochowitz

Corresponding Author

Dr. Zvi Borochowitz

Simon Winter Institute of Human Genetics, Bnai-Zion Medical Center, Technion-Faculty of Medicine, Haifa, Israel

Simon Winter Institute of Human Genetics, Bnai-Zion Medical Center, P.O. Box 4940, Haifa 31048, IsraelSearch for more papers by this author
Shimon Degani

Shimon Degani

Department of Obsterics and Gynecology, Bnai-Zion Medical Center, Technion-Faculty of Medicine, Haifa, Israel

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Hanna Dar

Hanna Dar

Simon Winter Institute of Human Genetics, Bnai-Zion Medical Center, Technion-Faculty of Medicine, Haifa, Israel

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Izu Ibschitz

Izu Ibschitz

Department of Obsterics and Gynecology, Bnai-Zion Medical Center, Technion-Faculty of Medicine, Haifa, Israel

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Mordechai Sharf

Mordechai Sharf

Department of Obsterics and Gynecology, Bnai-Zion Medical Center, Technion-Faculty of Medicine, Haifa, Israel

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First published: 1 June 1992
Citations: 44

Abstract

A diagnosis of the Neu-Laxova syndrome (NLS) was made by ultrasonography at 32 wks of gestation. Ultrasonographic examination showed intrauterine growth retardation (IUGR), Dandy-Walker anomaly, choroid plexus cysts, receding forehead and microcephaly, bilateral cataract without prominent eyes, scalp edema with no generalized edema, retrognathia, curved penis, and flexion deformities of limbs.

The findings in this case are consistent with NLS; however, they did not fit any of Curry's [1982] groups. Massive swelling of hands and feet were among the main manifestations in classic NLS cases. In the case presented herein, edema was noted only in the scalp. This might shed further light on the question of variability vs. heterogeneity in the NLS.

This case shows the existing possibility of an early diagnosis of NLS and adds Dandy-Walker anomaly and choroid plexus cysts as new findings to this syndrome. © 1992 Wiley-Liss, Inc.

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