𝔖 Bobbio Scriptorium
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Congenital Horner's syndrome does not alter Lisch nodule formation

✍ Scribed by Dr. Joel S. Mindel; Allan E. Rubenstein; Sibylle Wallace; Alan M. Aron; Jane Halperin


Book ID
101468968
Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
230 KB
Volume
35
Category
Article
ISSN
0364-5134

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✦ Synopsis


A 21-year-old woman with neurofibromatosis type 1 (NF-1) had a unilateral congenital Horner's syndrome with resultant hypopigmentation of the affected iris. Lisch nodules, which are melanocytic hamartornas, were similar in number, size, and pigmentation in both eyes. The present findings suggest that the formation of Lisch nodules is not influenced by the presence or absence of sympathetic innervation of the iris.