Abstract
According to criteria proposed by Voron et al., to diagnose LS, the patient must have lentiginosis along with at least two of the minor criteria, which are cardiac structural or ECG abnormalities, genitourinary abnormalities, endocrinal abnormalities, neurologic defects, cephalofacial dysmorphism, shortness of stature, skeletal abnormalities, and other cutaneous abnormalities. According to some authors, LS patients have increased melanocytic activity, secondary to an abnormal development of neural crest cells and increased β-adrenergic effector activity in the myocardium.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer