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CONTENTS TO VOLUME 1
DISORDERS OF HYPOP1GMENTATION
TUMORS CYSTS AND NEVI
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A.M.A. Arch abnormality absence acid acute affected alopecia areata amyloidosis anemia angioedema Angiokeratoma appear areas associated asymptomatic atrophy autosomal dominant autosomal dominant trait autosomal recessive basal cell BIBLIOGRAPHY blood bone Brit carcinoma changes characterized chronic clinical congenital Courtesy cutaneous Cutis cysts defect deficiency Definition Dermat develop Differential Diagnosis disease disorder edema epidermis erythema Erythropoietic Etiology Etiology-Inheritance extremities Fabry's disease females fibroblasts frequently genetic gingival glands growth hair hemochromatosis hemorrhagic hereditary hereditary hemorrhagic telangiectasia histological hypertrichosis idiopathic increased inheritance involved keloids keratoacanthoma keratoses lesions leukonychia lipodystrophy liver lymphedema males malignant manifestations mental metabolic monilethrix Mucopolysaccharidosis mucosa multiple nails nevus nodules normal occur oral pain papules Pathology patients Pediatrics percent pigmentation plasma porphyria cutanea tarda present at birth Prognosis rare reported retardation scalp serum sickle cell skin subcutaneous Symptoms syndrome Synonyms telangiectasia thalassemia therapy thickening tissue tongue transmitted Treatment tumors ulcers urine urticaria usually Variations-Complications xanthomas