Oculocutaneous albinism (OCA) is a congenital condition causing hypo pigmentation of the hair, skin, and eyes. Albinism and solar radiation are established risk factors for skin cancer, the commonest being squamous cell carcinoma (SCC) of the head and neck in black Africans. We present four OCA patients with histologic diagnosis of skin cancer presented to the University of Calabar Teaching Hospital from January, 2007 and December, 2008. These cases were compared with SCC and total skin malignancy seen during the same period. Forty-five patients presented skin malignancy during the study period. Four OCA patients (2 men and 2 women) with SCC accounted for 21.1 % of SCC and 8.9 % of skin malignancy. They ranged in age from 21 to 30 years (me...
Oculocutaneous Albinism (OCA) is a genetic condition in which individuals are born without pigmentat...
Although the majority of skin cancers in albino patients consists of squamous and basal cell carcino...
Oculocutaneous albinism (OCA) is an autosomal recessive syndromic and non-syndromic defect with defi...
Oculocutaneous albinism which is characterised by impaired melanin biosynthesis is the most common i...
Abstract Background Albinism is a genetic disorder characterized by lack of skin pigmentation. It ha...
Context: Albinism is an inherited disorder of hypopigmentation involving the skin, eyes, and hair. T...
Background: Skin cancers are a major risk associated with albinism and are thought to be a major cau...
A 32-year-old male with a history of albinism and farmer by occupation presented with an ulcerated p...
BACKGROUND Skin cancer is rare among Africans and albinism is an established risk for skin cancer...
Oculocutaneous albinism is a rare autosomal recessive disorder characterised by generalised depigmen...
Objective. The aim of this study was to study the histopathological patterns of skin lesions in pers...
The basal cell carcinoma is the most common skin tumour especially affecting the white individuals w...
Abstract Background Oculocutaneous albinism (OCA) is a genetically inherited autosomal recessive con...
Background. In Tanzania, squamous cell carcinoma (SCC) was the mostfrequent skin malignancy followed...
Oculocutaneous albinism is a genetically heterogeneous, autosomal recessive group of disorders chara...
Oculocutaneous Albinism (OCA) is a genetic condition in which individuals are born without pigmentat...
Although the majority of skin cancers in albino patients consists of squamous and basal cell carcino...
Oculocutaneous albinism (OCA) is an autosomal recessive syndromic and non-syndromic defect with defi...
Oculocutaneous albinism which is characterised by impaired melanin biosynthesis is the most common i...
Abstract Background Albinism is a genetic disorder characterized by lack of skin pigmentation. It ha...
Context: Albinism is an inherited disorder of hypopigmentation involving the skin, eyes, and hair. T...
Background: Skin cancers are a major risk associated with albinism and are thought to be a major cau...
A 32-year-old male with a history of albinism and farmer by occupation presented with an ulcerated p...
BACKGROUND Skin cancer is rare among Africans and albinism is an established risk for skin cancer...
Oculocutaneous albinism is a rare autosomal recessive disorder characterised by generalised depigmen...
Objective. The aim of this study was to study the histopathological patterns of skin lesions in pers...
The basal cell carcinoma is the most common skin tumour especially affecting the white individuals w...
Abstract Background Oculocutaneous albinism (OCA) is a genetically inherited autosomal recessive con...
Background. In Tanzania, squamous cell carcinoma (SCC) was the mostfrequent skin malignancy followed...
Oculocutaneous albinism is a genetically heterogeneous, autosomal recessive group of disorders chara...
Oculocutaneous Albinism (OCA) is a genetic condition in which individuals are born without pigmentat...
Although the majority of skin cancers in albino patients consists of squamous and basal cell carcino...
Oculocutaneous albinism (OCA) is an autosomal recessive syndromic and non-syndromic defect with defi...