Pigmentary anomalies in the multiple lentigines syndrome: Is it distinct from LEOPARD syndrome?

Pediatric Dermatology

Volumn 13, Issue 2, 1996, Pages 100-104

  Arnsmeier, Sheryl L ^a   Paller, Amy S ^a,b  

^a NORTHWESTERN UNIVERSITY   (United States)

^b CHILDREN'S MEMORIAL HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; DIFFERENTIAL DIAGNOSIS; FEMALE; GENETIC COUNSELING; HEARING LOSS; HEARING TEST; HEART DISEASE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPERPIGMENTATION; LENTIGO; MALE; MICROCEPHALY; PHYSICAL EXAMINATION; PIGMENT DISORDER; PRIORITY JOURNAL; SLIT LAMP; SYNDROME;

EID: 0029990055     PISSN: 07368046     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1525-1470.1996.tb01413.x     Document Type: Article

References (22)

1. Gorlin RJ, Anderson RC, Blaw M. Multiple lentigines syndrome. Am J Dis Child 1969;117:652-662.
2. Pipkin AC, Pipkin SB. A pedigree of generalized lentigo. J Hered 1950;41:79-82.
3. Tay CH, Rajagopala K, McEvoy-Bowe E, et al. A recessive disorder with growth and mental retardation, peculiar facies, abnormal pigmentation, hepatic cirrhosis and aminoaciduria. Acta Pædiatr Scand 1974;63:777-782.
4. Laude TA, Rajkumar SV, Russo RM, et al. Congenital lentiginosis. Cutis 1977,19:615-617.
5. Uhle P, Norvell SS. Generalized lentiginosis. J Am Acad Dermatol 1988;18:444-447.
6. Seuanez H, Mane-Garzon F, Kolski R. Cardiocutaneous syndrome (the LEOPARD syndrome). Review of the literature and a new family. Clin Genet 1976;9:266-276.
7. Polani PE, Moynahan EJ. Progressive cardiomyopathic lentiginosis. J Med 1972;162:205-225.
8. Selmanowitz VJ, Orentreich N, Felsenstein JM. Lentiginous profusa syndrome (multiple lentigines syndrome). Arch Dermatol 1971;104:393-401.
9. Walther RJ, Polansky BJ, Grots IA. Electrocardiographic abnormalities in a family with generalized lentigo. N Engl J Med 1966;275:1220-1225.
10. Nitelea OG, Dociu I. Lentiginoses et anomalies de développement. Dermatologica 1974;148:108-115.
11. Smith RF, Pulicchio LU, Holmes AV. Generalized lentigo: electrocardiographic abnormalities, conduction disorders and arrhythmias in three cases. Am J Cardiol 1970;25:501-506.
12. David LM. Multiple lentigines syndrome. Arch Dermatol 1973;108:590.
13. Maurice PDL, Breathnach SM. Multiple lentigines syndrome. Br J Dermatol 1988;119:115-116.
14. Apted JH. Multiple granular-cell myoblastoma (schwannoma) in a child. Br J Dermatol 1968;80:257-260.
15. Voron DA, Hatfield HH, Kalkhoff RK. Multiple lentigines syndrome. Am J Med 1976;60:447-456.
16. Korf BR. Diagnostic outcome in children with multiple café au lait spots. Pediatrics 1922;90:924-927.
17. Bats D, ed. Le syndrome LEOPARD. Amiens: Thèse Médicine, 1976:177.
18. Weiss LW, Zelickson AS. Giant melanosomes in multiple lentigines syndrome. Arch Dermatol 1977; 113:491-494.
19. Selmanowitz VJ. Lentiginosis profusa syndrome. IV. Giant pigment granules (light microscopy). Acta Dermatol 1975;55:481-484.
20. Fryer PR, Pope FM. Accumulation of membranebound melanosomes occurs in Langerhans cells of patients with the LEOPARD syndrome. Clin Exp Dermatol 1992;17:13-15.
21. Allegue F, Espana A, Fernandez-Garcia JM, et al. Segmental neurofibromatosis with contralateral lentiginosis. Clin Exp Dermatol 1989;14:448-450.
22. McKusick VA. Mendelian inheritance in man. Baltimore: Johns Hopkins Press, 1994:863-864.