02959nam 2200637Ia 450 991078505380332120230418175142.00-19-045328-10-19-997522-11-282-66139-697866126613960-19-977440-4(CKB)2670000000030277(EBL)547965(OCoLC)646820870(SSID)ssj0000418514(PQKBManifestationID)11267101(PQKBTitleCode)TC0000418514(PQKBWorkID)10371552(PQKB)10624812(StDuBDS)EDZ0000105577(MiAaPQ)EBC547965(Au-PeEL)EBL547965(CaPaEBR)ebr10399397(CaONFJC)MIL266139(EXLCZ)99267000000003027720090506d2010 uy 0engur|n|---|||||txtrdacontentcrdamediacr rrdacarrierGenetic skin disorders /Virginia P. SybertSecond edition.Oxford ;New York :Oxford University Press,2010.1 online resource (785 pages) illustrationsOxford monographs on medical genetics ;no. 60Description based upon print version of record.0-19-539766-5 Includes bibliographical references and index.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; IndexThis 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.Oxford monographs on medical genetics ;60.SkinDiseasesGenetic aspectsDermatologySkinDiseasesGenetic aspects.Dermatology.616.5/042Sybert Virginia P1171501MiAaPQMiAaPQMiAaPQBOOK9910785053803321Genetic skin disorders2725891UNINA