Atlas of GenodermatosesA lavishly illustrated guide to almost 200 inherited diseases of the skin, hair, and nails. Each entry includes synonyms, age of onset, clinical findings, complications, course, laboratory findings, diagnosis, therapy, and key references, adding up to far more than just a collection of photographs. In addition to being a clinical primer, this is also a work of scientific research and contains the first printed description of two new syndromes. The fast-moving world of genetic research means that the latest genetic correlations, included here, render previous texts out of date. All specialists in Dermatology and Pediatrics should find this an invaluable front-line resource in the clinic. |
Contents
Epidermolysis bullosa | 1 |
Epidermolytic hyperkeratoses | 17 |
Acantholytic diseases | 29 |
Ichthyoses | 37 |
Erythrokeratodermas | 67 |
Other disorders of keratinization | 93 |
Poikilodermas and aging syndromes | 107 |
Hair diseases | 123 |
Disorders of pigmentation | 275 |
Vascular disorders | 297 |
Metabolic disease | 327 |
Immunodeficiency disorders | 345 |
Complex malformative syndromes with distinctive cutaneous signs | 351 |
Genodermatoses related to malignancy | 367 |
Cutaneous mosaicism | 393 |
19 | 394 |
Nail disorders | 151 |
Sebocystomatosis | 161 |
Neurocutaneous syndromes | 171 |
Ectodermal dysplasias and related disorders | 203 |
Fatty tissue anomalies | 233 |
Disorders of connective tissue | 239 |
Aplasia cutis | 269 |
29 | 402 |
407 | |
409 | |
415 | |
421 | |
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Common terms and phrases
abnormalities Acad Dermatol Age of onset alopecia anomalies Arch Dermatol areas atrophic Autosomal dominant Autosomal dominant inheritance autosomal recessive birth Clinical findings bone café-au-lait spots chromosome Clin Clinical findings Cutaneous congenital Course and complications Course and prognosis cysts defects Differential diagnosis dystrophy ectodermal dysplasia Ehlers-Danlos syndrome encoding Epidemiology Epidemiology The disease epidermolytic epidermolytic hyperkeratosis erythematous Extracutaneous findings Extracutaneous manifestations Extracutaneous symptoms Familial Figure findings Cutaneous manifestations follicular Follow-up and therapy gene Genetics and pathogenesis hair shaft Happle Hum Genet hyperhidrosis hyperkeratosis hypertrichosis ichthyosis Incontinentia pigmenti infections Invest Dermatol involvement keratin keratolytic Keratosis Laboratory findings Laboratory investigations lesions linear malformations malignant melanocytes mental retardation molecular mosaic mucosa mutations nail Neurological nevi nevus syndrome Oral retinoids palmoplantar keratoderma papules pathogenesis The disease patients pattern Pediatr Dermatol Phakomatosis phenotype pigmented progressive protein Proteus syndrome rare REFERENCES reported retinoids scalp severe skin sporadic syndrome Age syndrome Epidemiology SYNDROME Synonym tissue tumors visible X-linked