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Items: 1 to 20 of 126

1.

Phylloid pattern of hypomelanosis closely related to chromosomal abnormalities in the 13q detected by SNP array analysis.

Faletra F, Berti I, Tommasini A, Pecile V, Cleva L, Alberini E, Bruno I, Gasparini P.

Dermatology. 2012;225(4):294-7. doi: 10.1159/000342884. Epub 2012 Oct 24.

2.

Phylloid hypomelanosis is closely related to mosaic trisomy 13.

Happle R.

Eur J Dermatol. 2000 Oct-Nov;10(7):511-2.

PMID:
11056419
3.

Phylloid hypomelanosis and mosaic partial trisomy 13: two cases that provide further evidence of a distinct clinicogenetic entity.

González-Enseñat MA, Vicente A, Poo P, Catalá V, Mar Pérez-Iribarne M, Fuster C, Geán E, Happle R.

Arch Dermatol. 2009 May;145(5):576-8. doi: 10.1001/archdermatol.2009.37.

PMID:
19451503
4.

Tetrasomy 13q mosaicism associated with phylloid hypomelanosis and precocious puberty.

Dhar SU, Robbins-Furman P, Levy ML, Patel A, Scaglia F.

Am J Med Genet A. 2009 May;149A(5):993-6. doi: 10.1002/ajmg.a.32758.

5.
6.

Phylloid pattern of pigmentary disturbance in a case of complex mosaicism.

Ribeiro Noce T, de Pina-Neto JM, Happle R.

Am J Med Genet. 2001 Jan 15;98(2):145-7.

PMID:
11223850
7.

Mosaic tetrasomy 13q and phylloid hypomelanosis: a case report and review of the literature.

Myers JN Jr, Davis L, Sheehan D, Kulharya AS.

Pediatr Dermatol. 2015 Mar-Apr;32(2):263-6. doi: 10.1111/pde.12375. Epub 2014 Jun 12. Review.

PMID:
24920397
8.

Phylloid pigmentary pattern with mosaic trisomy 13.

Horn D, Rommeck M, Sommer D, Körner H.

Pediatr Dermatol. 1997 Jul-Aug;14(4):278-80.

PMID:
9263307
9.

Hypomelanosis of ito with trisomy 13 mosaicism [46, XY, der (13;13) (q10;q10), +13/46,xy].

Yakinci C, Kutlu NO, Alp MN, Senol M, Durmaz Y, Budak T.

Turk J Pediatr. 2002 Apr-Jun;44(2):152-5.

PMID:
12026206
10.

[Hypomelanosis of Ito in a girl with Trisomy 13 mosaicism: a cytogenetic study].

Ronger S, Till M, Kanitakis J, Balme B, Thomas L.

Ann Dermatol Venereol. 2003 Nov;130(11):1033-8. Review. French.

PMID:
14724538
11.

Phylloid hypermelanosis and melanocytic nevi with aggregated and disfigured melanosomes: causal relationship between phylloid pigment distribution and chromosome 13 abnormalities.

Oiso N, Tsuruta D, Imanishi H, Sayasa H, Narita T, Kobayashi H, Ikegami H, Kawada A.

Dermatology. 2010;220(2):169-72. doi: 10.1159/000277273. Epub 2010 Jan 26. Review.

PMID:
20110628
12.

Celiac disease, phylloid hypomelanosis and autoimmune thyroiditis: a case report.

Tosun MS, Ertekin V.

Turk J Pediatr. 2015 Nov-Dec;57(6):639-641.

PMID:
27735809
13.

Dohi Memorial Lecture. New aspects of cutaneous mosaicism.

Happle R.

J Dermatol. 2002 Nov;29(11):681-92.

PMID:
12484429
14.

Prenatal diagnosis and genetic counseling for mosaic trisomy 13.

Chen CP.

Taiwan J Obstet Gynecol. 2010 Mar;49(1):13-22. doi: 10.1016/S1028-4559(10)60003-4. Review.

15.

Patau syndrome with long survival in a case of unusual mosaic trisomy 13.

Fogu G, Maserati E, Cambosu F, Moro MA, Poddie F, Soro G, Bandiera P, Serra G, Tusacciu G, Sanna G, Mazzarello V, Montella A.

Eur J Med Genet. 2008 Jul-Aug;51(4):303-14. doi: 10.1016/j.ejmg.2008.03.004. Epub 2008 Apr 9.

PMID:
18495567
16.

Total Hemi-overgrowth in Pigmentary Mosaicism of the (Hypomelanosis of) Ito Type: Eight Case Reports.

Pavone V, Signorelli SS, Praticò AD, Corsello G, Savasta S, Falsaperla R, Pavone P, Sessa G, Ruggieri M.

Medicine (Baltimore). 2016 Mar;95(10):e2705. doi: 10.1097/MD.0000000000002705. Erratum in: Medicine (Baltimore). 2016 Apr;95(15):e80ef. Ba, Martino Ruggieri [Corrected to Ruggieri, Martino].

17.

New association between ring chromosome 20 syndrome and hypomelanosis of Ito.

Cappanera S, Passamonti C, Zamponi N.

Pediatr Neurol. 2011 Nov;45(5):341-3. doi: 10.1016/j.pediatrneurol.2011.08.006.

PMID:
22000318
18.

Pigmentary abnormalities in trisomy of chromosome 13.

Pillay T, Winship WS, Ramdial PK.

Clin Dysmorphol. 1998 Jul;7(3):191-4.

PMID:
9689992
19.

Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report.

Ponti G, Pellacani G, Tomasi A, Percesepe A, Guarneri C, Guerra A, Mandel VD, Kisla E, Cevikel P, Neri C, Menozzi C, Seidenari S.

J Med Case Rep. 2014 Oct 9;8:333. doi: 10.1186/1752-1947-8-333.

20.

Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes.

Taibjee SM, Bennett DC, Moss C.

Br J Dermatol. 2004 Aug;151(2):269-82. Review.

PMID:
15327534

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