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  Vol. 21 No. 3, September 1969 TABLE OF CONTENTS
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Two Unusual Neurocutaneous Disorders With Facial Cutaneous Signs

Gerald I. Sugarman, MD; William B. Reed, MD

Arch Neurol. 1969;21(3):242-247.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

CUTANEOUS lesions of the face frequently are signs of associated cerebral or neurological disease. Well-known examples are tuberous sclerosis, Klein-Waardenberg syndrome, Sturge-Weber-Demitri syndrome, and to a lesser extent, facial hemiatrophy (Romberg-Parry syndrome). We would like to report two cases in which cutaneous signs were associated with severe mental deficiency and epilepsy. One patient had a nevus sebaceous of the mixed type, and the other had a cutaneous segmental depigmentation of the face, not previously described in the literature.

Report of Cases

CASE 1.—A 12-year-old Chinese girl was seen in 1967 at the Childrens Hospital Clinical Research Center. At that time, she had been institutionalized for ten years at Pacific State Hospital for profound mental retardation.

History.—

The patient was the third child of a 26-year-old Chinese woman who had had a normal pregnancy, labor, and delivery. The child weighed 2,978 gm (6 lb 9 ounces) at birth. Head circumference, . . . [Full Text PDF of this Article]


Author Affiliations

Los Angeles

From the Division of Neurology, Childrens Hospital of Los Angeles, University of Southern California (Dr. Sugarman), and the Department of Dermatology, University of California School of Medicine (Dr. Reed), Los Angeles.


Footnotes

Submitted for publication March 12, 1969; accepted March 29.

Reprint requests to 3325 Division St, Los Angeles 90065 (Dr. Sugarman).



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