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Congenital Deafness and Multiple LentiginesA Report of Cases in a Mother and Daughter
Arnold J. Capute, MD;
David L. Rimoin, MD, PhD;
Bruce W. Konigsmark, MD;
Nancy B. Esterly, MD;
Frederick Richardson, MD
Arch Dermatol. 1969;100(2):207-213.
Abstract
A kindred is presented in which an adolescent female and a mother are affected with profound hearing loss and generalized lentigines. This combination of lesions comprises a distinct syndrome probably inherited as a dominant trait and appears to be different from other syndromes involving deafness and pigmentary lesions.
Author Affiliations
Baltimore; St. Louis; Baltimore
From The Johns Hopkins School of Medicine and The John F. Kennedy Institute for Habilitation of the Mentally and Physically Handicapped Child, Baltimore (Dr. Capute); the Washington University School of Medicine, St. Louis (Dr. Rimoin); The Johns Hopkins School of Medicine (Drs. Konigsmark and Esterly); and the Department of Pediatrics, The Johns Hopkins School of Medicine and The John F. Kennedy Institute for Habilitation of the Mentally and Physically Handicapped Child (Dr. Richardson). Dr. Esterly is currently at the LaRabida-University of Chicago Institute, The University of Chicago.
Footnotes
Accepted for publication March 4, 1969.
Reprint requests to Department of Pediatrics, The Johns Hopkins School of Medicine, 707 N Broadway, Baltimore 21205 (Dr. Capute).
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