Donor dominance cures CHILD nevus

Dermatology

Volumn 220, Issue 4, 2010, Pages 340-345

  König, Arne ^a   Skrzypek, Jan ^a   Löffler, Harald ^b   Oeffner, Frank ^a   Grzeschik, Karl Heinz ^a   Happle, Rudolf ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

^b SLK Kliniken Heilbronn   (Germany)

Author keywords

Congenital hemidysplasia with ichthyosiform nevus and limb defects; Dermabrasion; Lateralization; Lyonization; NSDHL mutations; Split skin grafts

Indexed keywords

CEFUROXIME; 3(OR 17)BETA HYDROXYSTEROID DEHYDROGENASE; NSDHL PROTEIN, HUMAN; STOP CODON;

ADULT; ARTICLE; BIRTH DEFECT; CASE REPORT; CHILD; CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM NEVUS AND LIMB DEFECT SYNDROME; DONOR; ESTHETIC SURGERY; FEMALE; FOLLOW UP; FULL THICKNESS SKIN GRAFT; HUMAN; MALE; MUTATIONAL ANALYSIS; NAIL BED; NAIL DYSTROPHY; NONSENSE MUTATION; PLASTIC SURGERY; PRESCHOOL CHILD; PRIORITY JOURNAL; REMISSION; SCHOOL CHILD; SKIN ABRASION; SKIN BIOPSY; SPLIT THICKNESS SKIN GRAFT; SURGICAL APPROACH; TREATMENT DURATION; TREATMENT OUTCOME; X CHROMOSOME; X CHROMOSOME LINKED DISORDER; FINGER; GENETIC DISEASES, X-LINKED; GENETICS; ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL; LIMB DEFORMITIES, CONGENITAL; NEVUS; PROCEDURES; SKIN NEOPLASMS; SKIN TRANSPLANTATION; STOP CODON; SYNDROME;

3-HYDROXYSTEROID DEHYDROGENASES; ADULT; CHILD; CODON, NONSENSE; FEMALE; FINGERS; GENETIC DISEASES, X-LINKED; HUMANS; ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL; LIMB DEFORMITIES, CONGENITAL; NEVUS; SKIN NEOPLASMS; SKIN TRANSPLANTATION; SYNDROME; TREATMENT OUTCOME;

EID: 77954244610     PISSN: 10188665     EISSN: None     Source Type: Journal    
DOI: 10.1159/000287253     Document Type: Article

References (9)

1. Happle R, Mittag H, Küster W: The CHILD nevus: a distinct skin disorder. Dermatology 1995; 191: 210-216.
2. Happle R, Koch H, Lenz W: The CHILD syndrome: congenital hemidysplasia with ichthyosiform erythroderma and limb defects. Eur J Pediatr 1980; 134: 27-33.
3. König A, Happle R, Bornholdt D, Engel H, Grzeschik KH: Mutations in the NSDHL gene, encoding a 3beta-hydroxysteroid dehydrogenase, cause CHILD syndrome. Am J Med Genet 2000; 90: 339-346.
4. König A, Happle R, Bornholdt D, Engel H, Grzeschik KH: A novel missense mutation of NSDHL in an unusual case of CHILD syndrome showing bilateral, almost symmetrical involvement. J Am Acad Dermatol 2002; 46: 594-596.
5. Hummel M, Cunningham D, Mullett CJ, Kelley RI, Herman GE: Left-sided CHILD syndrome caused by a nonsense mutation in the NSDHL gene. Am J Med Genet A 2003; 122A:246-251.
6. Bornholdt D, König A, Happle R, Leveleki L, Bittar M, Danarti R, Vahlquist A, Tilgen W, Reinhold U, Poiares Baptista A, Grosshans E, Vabres P, Niiyama S, Sasaoka K, Tanaka T, Meiss AL, Treadwell PA, Lambert D, Camacho F, Grzeschik KH: Mutational spectrum of NSDHL in CHILD syndrome. J Med Genet 2005; 42:e17.
7. Kim CA, König A, Bertola DR, Albano LM, Gattas GJ, Bornholdt D, Leveleki L, Happle R, Grzeschik KH: CHILD syndrome caused by a deletion of exons 6-8 of the NSDHL gene. Dermatology 2005; 211: 155-158.
8. Happle R, Effendy I, Megahed M, Orlow SJ, Küster W: CHILD syndrome in a boy. Am J Med Genet 1996; 62: 192-194.
9. Fink-Puches R, Soyer HP, Pierer G, Kerl H, Happle R: Surgical treatment of CHILD nevus. Eur J Dermatol 2000; 10: 262-264.