Hypermelanoses of the Newborn and of the Infant

Dermatologic Clinics

Volumn 25, Issue 3, 2007, Pages 327-336

  Taïeb, Alain ^a   Boralevi, Franck ^a,b  

^a BORDEAUX UNIVERSITY HOSPITAL   (France)

^b HÔPITAL PELLEGRIN   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BLUE NEVUS; CAFE AU LAIT SPOT; CLINICAL FEATURE; CONGENITAL NEVUS; DIFFERENTIAL DIAGNOSIS; DISEASE CLASSIFICATION; HAMARTOMA; HUMAN; INFANT; LENTIGINOSIS; LENTIGO; MELANOCYTOSIS; MELANOSIS; MONGOLIAN SPOT; NEWBORN; OTA NEVUS; PRIORITY JOURNAL; REVIEW; SCROTUM; SKIN COLOR; SYNDROME DELINEATION;

CAFE-AU-LAIT SPOTS; DIAGNOSIS, DIFFERENTIAL; HUMANS; HYPERPIGMENTATION; INFANT; INFANT, NEWBORN; LENTIGO; MEDICAL HISTORY TAKING; MELANOSIS; MONGOLIAN SPOT; NEVUS; PHYSICAL EXAMINATION; SKIN NEOPLASMS;

EID: 34447643207     PISSN: 07338635     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.det.2007.04.011     Document Type: Review

References (20)

1. Lamason R.L., Mohideen M.A., Mest J.R., et al. SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans. Science 310 5755 (2005) 1782-1786
2. Newton J.M., Cohen-Barak O., Hagiwara N., et al. Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4. Am J Hum Genet 69 (2001) 981-988
3. Suzuki N., Suzuki T., Inagaki K., et al. Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis. J Invest Dermatol 124 6 (2005) 1186-1192
4. Crespel E., Plantin P., Schoenlaub P., et al. Hyperpigmentation of the distal phalanx in healthy Caucasian neonates. Eur J Dermatol 11 2 (2001) 120-121
5. nd edition (2006), Blackwell Publishing Ltd, Oxford (UK) 55-65
6. Alper J., Holmes L.B., and Mihm Jr. M.C. Birthmarks with serious medical significance: nevocellular nevi, sebaceous nevi, and multiple cafe-au-lait spots. J Pediatr 95 (1979) 696-700
7. Crowe F.W., Schull W.J., and Neel J.V. A clinical, pathological and genetic study of multiple neurofibromatosis (1956), Charles C Thomas, Springfield (IL)
8. Korf B.R. Diagnostic outcome in children with multiple cafe au lait spots. Pediatrics 90 6 (1992) 924-927
9. Abeliovich D., Gelman-Kohan Z., Silverstein S., et al. Familial cafe au lait spots: a variant of neurofibromatosis type 1. J Med Genet 32 (1995) 985-986
10. Weinstein L.S., Shenker A., Gejman P.V., et al. Activating mutations of the stimulatory G protein in the McCune-Albright syndrome. N Engl J Med 325 (1991) 1688-1695
11. Benedict P.H., Szabo G., Fitzpatrick T.B., et al. Melanotic macules in Albright's syndrome and in neurofibromatosis. JAMA 205 9 (1968) 618-628
12. Gelb B.D., and Tartaglia M. Noonan syndrome and related disorders: dysregulated RAS-mitogen activated protein kinase signal transduction. Hum Mol Genet 15 Suppl 2 (2006) R220-R226
13. Taïeb A, Vergnes P. Naevus congénitaux. In: Lorette G, Lacour JP, editors. Progrès en pédiatrie. Paris: Doin; in press.
14. Claudel P., Labbe L., Pedespan J.M., et al. Linear and whorled nevoid hypermelanosis: report of two cases. Arch Pediatr 5 10 (1998) 1098-1102
15. Jenne D.E., Reimann H., Nezu J., et al. Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase. Nat Genet 18 1 (1998) 38-43
16. Boikos S.A., and Stratakis C.A. Carney complex: pathology and molecular genetics. Neuroendocrinology 83 3-4 (2006) 189-199
17. Ashrafi M.R., Shabanian R., Mohammadi M., et al. Extensive mongolian spots: a clinical sign merits special attention. Pediatr Neurol 34 2 (2006) 143-145
18. Zhang C., Deng Y., Chen X., et al. Linkage of a locus determining familial progressive hyperpigmentation (FPH) to chromosome 19p13.1-pter in a Chinese family. Eur J Dermatol 16 3 (2006) 246-250
19. Ruiz-Maldonado R., Tamayo L., and Fernandez-Diez J. Universal acquired melanosis: the carbon baby. Arch Dermatol 114 5 (1978) 775-778
20. Bertini G., Dani C., Fonda C., et al. Bronze baby syndrome and the risk of kernicterus. Acta Paediatr 94 7 (2005) 968-971