multiple lentigines syndrome…

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pectus excavatum, leopard syndrome, multiple lentigines syndrome, inherited disorder identified, increased number of lentigines, freckle-like spots, multiple lentigines syndrome is inherited, an autosomal dominant trait, people have large numbers of lentigines, present from birth, somewhat darker than true freckles, the most obvious sign, located mostly on the trunk, neck, people, wide-set eyes, hypertelorism, prominent ears, nerve deafness, partial, cafe-au-lait spots, light brown birthmarks, additional findings include mild pulmonic stenosis, in the ecg, electrocardiogram, have abnormal genitalia, cryptorchidism, hypogonadism, delayed puberty, a family history of multiple lentigines, multiple lentigines on neck, trunk, on any cutaneous surface, cafe-au-lait spots, wide-set eyes, hypertelorism, prominent ears, pectus excavatum, pectus carinatum, abnormalities, the sternum, breastbone, undescended testicles, cryptorchidism, slow growth, delayed puberty, absent puberty, a physical examination, signs of mild pulmonic stenosis, obstruction, the pulmonic heart valve, obstructive cardiomyopathy, ecg, abnormalities, hearing test, endocrine evaluation, treatment is directed toward the correctable problems, degree of hearing loss must be determined, hearing aids supplied, action, be necessary, expected time of puberty to cause the normal changes to occur, most patients adjust very well, proper attention to specific problems, complications, variable, deafness, delayed puberty, heart problems, infertility, symptoms of this disorder, family history of this disorder, plan to have children, genetic counseling, a family history of multiple lentigines syndrome who want to have children.