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PRINCIPLES OF GENE EXPRESSION AND HEREDITY
DISORDERS OF HYPOPIGMENTATION
TUMORS CYSTS AND NEVI
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abnormalities acanthosis nigricans affected individuals albinism alopecia appear Arch areas associated atrophy autosomal dominant autosomal recessive BIBLIOGRAPHY bullae bullous cell changes characterized chromosome clinical collagen Complications congenital ichthyosiform erythroderma cutaneous cutis laxa cutis verticis gyrata defects deficiency Dermat develop Differential Diagnosis disorder Dyskeratosis ectodermal dysplasia Ehlers-Danlos syndrome epidermis epidermolysis bullosa Etiology extremities females follicular freckles frequently gene genetic hair hereditary histological horny hyperhidrosis hyperkeratosis hypoplasia Ichthyosis linearis circumflexa ichthyosis vulgaris incontinentia pigmenti increased Inheritance involved keratosis follicularis keratosis palmoplantaris keratosis pilaris keratotic lesions macules males manifestations membrane mental retardation mucosa nails neurofibromatosis nevus normal noted occur ocular palms and soles papules Pathology patients percent pigmentation Pityriasis rubra pilaris plaques porokeratosis present at birth Prognosis Pseudoxanthoma elasticum rare recessive trait Recklinghausen's disease reported scalp scarring sexes skin Symptoms Synonyms thickened tissue Treatment tuberous sclerosis tumors ulcers usually Variations vitamin A acid vitiligo Werner's syndrome X-linked