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Clinical Picture
Neal P. Simon, MD;
Michael W. Simon, MD;
Walter W. Tunnessen, Jr, MD
Arch Fam Med. 1997;6(5):419-420.
References
Article references have been provided for searching and linking. Additional reference information may be available in the article PDF.
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1. Hurwitz S. Clinical Pediatric Dermatology. Philadelphia, Pa: WB Saunders Co; 1993:466-467.
2. Smith DW. Waardenburg syndrome, types I and II. In: Jones KL, ed. Smith's Recognizable Patterns of Human Malformation. Philadelphia, Pa: WB Saunders Co; 1988:208-209. 3. Bolognia JL, Pawelek JM. Biology of hypopigmentation. J Am Acad Dermatol. 1988;19:217-255.
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4. Mallory SB, Wiener E, Nordlund JJ. Waardenburg's syndrome with Hirschsprung's disease: a neural crest defect. Pediatr Dermatol. 1986;3:119-124.
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5. Khaldi F, Serbegi M, Mokadem H, Lazzem B, Bennaceur B. Waardenburg syndrome: report of a familial case. Ann Pediatr (Paris). 1990;37:55-58.
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6. Hildesheimer M, Maayan Z, Muchnik C, Rubinstein M, Goodman RM. Auditory and vestibular findings in Waardenburg's type II syndrome. J Laryngol Otol. 1989;103:1130-1133.
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7. Harfi HA, Brismar J, Hainau B, Sabbah R. Partial albinism, immunodeficiency, and progressive white matter disease: a new primary immunodeficiency. Allergy Proc. 1992;13:321-328.
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8. Griscelli C, Durandy A, Guy-Grand D, Daguillard F, Herzog C, Prunieras M. A syndrome associating partial albinism and immunodeficiency. Am J Med. 1978;65:691-702.
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9. Brismar J, Harfi HA. Partial albinism with immunodeficiency: a rare syndrome with prominant posterior fossa white matter changes. AJNR Am J Neuroradiol. 1992;13:387-393.
ABSTRACT
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