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[null,"1.","Record Nr.",null,"UNINA9910459205903321"]
[null,null,"Autore",null,"Sybert Virginia P"]
[null,null,"Titolo",null,"Genetic skin disorders [[electronic resource] /] / Virginia P. Sybert"]
[null,null,"Pubbl/distr/stampa",null,"Oxford ; ; New York, : Oxford University Press, 2010"]
[null,null,"ISBN",null,"0-19-045328-1"]
[{"$nulls":4},"0-19-997522-1"]
[{"$nulls":4},"1-282-66139-6"]
[{"$nulls":4},"9786612661396"]
[{"$nulls":4},"0-19-977440-4"]
[null,null,"Edizione",null,"[2nd ed.]"]
[null,null,"Descrizione fisica",null,"1 online resource (785 p.)"]
[null,null,"Collana",null,"Oxford monographs on medical genetics ; ; no. 60"]
[null,null,"Disciplina",null,"616.5/042"]
[null,null,"Soggetti",null,"Skin - Diseases - Genetic aspects"]
[{"$nulls":4},"Dermatology"]
[{"$nulls":4},"Electronic books."]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Description based upon print version of record."]
[null,null,null,"Nota di bibliografia","Includes bibliographical references and index."]
[null,null,"Nota di contenuto",null,"Contents; Preface; Acknowledgments; Introduction; 1. PRACTICAL INHERITANCE; 2. DISORDERS OF THE EPIDERMIS: DIFFERENTIATION AND KINETICS; 3. DISORDERS OF EPIDERMAL APPENDAGES; 4. DISORDERS OF PIGMENTATION; 5. DISORDERS OF THE DERMIS; 6. DISORDERS OF SUBCUTANEOUS TISSUE; 7. LYMPHEDEMA; 8. URTICARIA; 9. OTHER DISORDERS; 10. TUMORS/HAMARTOMAS; 11. METABOLIC DISEASE; 12. PREMATURE AGING; 13. PHOTOSENSITIVITY; 14. IMMUNE DEFICIENCY DISEASES; Appendix A: Glossary; Appendix B: Differential Diagnosis by Skin Sign; Figure Credits; Index"]
[null,null,null,"Sommario/riassunto","This valuable text represents a comprehensive survey of well over 300 distinct inherited dermatologic conditions. Each disease entry follows a consistent format, allowing the clinician to quickly scan and access key information for differential diagnosis. Each entry contains sections devoted to dermatologic features, associated clinical abnormalities, histopathology, biochemical and molecular information, treatment, mode of inheritance and recurrence risk, prenatal diagnosis, and information on differential diagnosis. In addition the author has included support group listings and detailed anno"]