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Macromelanosomes in X-linked ocular albinism (XLOA)

Yoshiike, T.; Manabe, M.; Hayakawa, M.; Ogawa, H.

Acta Dermato-Venereologica 65(1): 66-69

1985

ISSN/ISBN: 0001-5555
PMID: 2578709
Document Number: 258430
A case of X-linked ocular albinism is reported. Characteristic Masson-Fontana positive and Dopa positive giant melanin granules were found in keratinocytes, melanocytes and upper dermis. Ultrastructurally the macromelanosome was composed of a dense core and a less dense surrounding mantle.

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Walker, B.A.; Martyn, L.J.; Coffman, T. 1971: X-linked ocular albinism Birth Defects Original Article Series 7(3): 200-202
Hayakawa, M.; Kanai, A.; Kato, K.; Nakajima, A.; Takamori, K. 1990: A Japanese family of Nettleship Falls X-linked ocular albinism Nippon Ganka Gakkai Zasshi 94(12): 1181-1187
Awaya, S.; Tsunekawa, F.; Koizumi, E.; Miyake, Y.; Yokoyama, K. 1988: Studies of X-linked recessive ocular albinism of the Nettleship-Falls type--with special reference to the association of megalocornea Nippon Ganka Gakkai Zasshi 92(1): 146-150
Krejcí, L.; Rodný, S. 1983: Atypical form of ocular albinism with a disorder of color perception Ceskoslovenska Oftalmologie 39(1): 25-28
Rodrigues, M.; Streett, R.P.; Highman, B. 1971: Partial ocular albinism in Mystromys albicaudatus (African white-tailed rat) Archives of Pathology 92(3): 212-218
Hou, J.-W. 2005: Detection of gene deletions in children with chondrodysplasia punctata, ichthyosis, Kallmann syndrome, and ocular albinism by FISH studies Chang Gung Medical Journal 28(9): 643-650
Rodríguez-Agramonte, F.; Izquierdo, N.J.; Cadilla, C. 2013: Ocular findings in patients with oculocutaneous albinism type ia with G47D tyrosinase gene mutation in Puerto Rico: a case report Boletin de la Asociacion Medica de Puerto Rico 105(2): 62-64
Gragg, G.W. 1971: Albinoidism and albinism Birth Defects Original Article Series 7(3): 203-204
Zhang, C.; Zhu, S.; Zhang, Y. 2000: X-linked thin basement membrane nephropathy was linked with COL4A5 gene Zhonghua Yi Xue Za Zhi 80(8): 582-584
Golding, B.; Golding, H.; Foiles, P.G.; Morton, J.I. 1983: CBA/N X-linked defect delays expression of the Y-linked accelerated autoimmune disease in BXSB mice Journal of Immunology 130(3): 1043-1046
Perry, P.K.; Silverberg, N.B. 2001: Cutaneous malignancy in albinism Cutis 67(5): 427-430
Predo'scu, V.; Christodorescu, D. 1972: Sex-linked (X-linked) heredity in mental and neurological diseases Neurologia Psihiatria Neurochirurgia 17(5): 441-452
Aquaron, R. 1980: Oculocutaneous albinism in Cameroun. About 216 cases Revue d'Epidemiologie et de Sante Publique 28(1): 81-88
Jung, E.G.; Anton-Lamprecht, I. 1971: Investigation of a case of oculocutaneous albinism Birth Defects Original Article Series 7(8): 26-30
Ferguson, F.G.; Irving, G.W.; Stedham, M.A. 1979: Three variations of hairlessness associated with albinism in the laboratory rat Laboratory Animal Science 29(4): 459-464
Hori, Y. 1978: Albinism--with special reference to its etiology Nihon Rinsho. Japanese Journal of Clinical Medicine Suppl: 2386-2387
Kalachev, I.I.; Mozherenkov, V.P. 1989: Albinism in the practice of ophthalmology (review of the literature) Vestnik Oftalmologii 105(2): 71-74
Rozsíval, P.; Cigánek, L. 1978: Subjective ocular functions and objective ocular symptomatology following large doses of atropine Ceskoslovenska Oftalmologie 34(6): 409-412
Chiou, G.C.; Chen, Y.J. 1992: Improvement of ocular blood flow with dopamine antagonists on ocular-hypertensive rabbit eyes Zhongguo Yao Li Xue Bao 13(6): 481-484
Basinskiĭ, S.N.; Cherkasova, I.N. 1984: Indices of ocular hemodynamics in patients with essential ocular hypertension Vestnik Oftalmologii 4: 16-18