20th World Congress of Dermatology
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Poster abstracts Monday 1st July - Tuesday 2nd July 2002 Genodermatoses P0653 Dupuytren's contracture and genaralized fibromatous plaques: a possibly new autosomal recessive disorder but with delayed onset P0654 Computer-associated diagnosis of genodermatoses P0655 Xeroderma pigmentosum: a case report P0656 Ectodermal dysplasia (two cases reported) P0657 Laser capture microdissection in the analysis of a mouse model for epidermolytic hyperkeratosis P0658 Neurofibromatosis type 1: clinical findings from a brazilian reference center P0659 Phacomatosis pigmentokeratotica P0660 TGM1 mutations in a hungarian patient with congenital ichthyosiform erythroderma P0661 Keratosis lichenoides chronica kaposi-N?kam P0662 Bilateral segmental neurofibromatosis with partial unilateral lentiginosis: two disease syndromes linked genetically? P0663 Happle's acantholytic ectodermal dysplasia. a new skin fragility syndrome P0664 Nevus telangiectaticus associated with nevus anemicus: nevus vascularis mixtus P0665 The porphyries: algerian experiment P0666 About three observations of continual skin peeling syndrome P0667 K.I.D syndrome: a cause of pachydermatoglyphia P0668 Systemic chemotherapy by fluorouracil-folinic acid in facial carcinomas secondary to xeroderma pigmentosum P0669 Olmsted syndrome and verrucous carcinoma P0670 Dyskeratosis follicularis Darier's: a case report P0671 Gastromy feeding in severe epidermolysis bullosa P0672 Syndrome of recurrent skin ulcerations, arthroosteolysis, keratitis, oligodontia and mental retardation P0673 Novel mutation of keratin 9 in a hungarian family with palmoplantar epidermolytic hyperkeratosis P0674 Pitiriasis rotunda: a clinical case presentation P0675 Punctate parakeratotic palmoplantar keratoderma P0676 An unusual presentation of incontinentia pigmenti P0677 A family with a syndrome of Waardenburg P0678 Genealogical studies and geographical distribution of dermatological diseases in the French Canada population of the Quebec province, Canada P0679 Mal de Meleda responsive to topical calcipotriol P0680 Pachyonychia congenita P0681 Perianal porokeratosis of Mibelli associated with vitiligo and autoimmune hypothyroidism P0682 Usefulness of skin echography for the non-invasive diagnosis of neurofibromas presenting as blue macules P0683 Cockayne syndrome: a report of five case studies P0684 Muir-Torre syndrome. A case report P0685 Kindler syndrome: A family in Chiapas P0686 Diagnose genodermatoses through evidence-based medicine P0687 Costello syndrome P0688 A new case of Hutchinson-Gilford progeria syndrome P0689 Tuberous sclerosis: treatment of facial angiofibromas by cryosurgery P0690 Incontinentia pigmenti P0691 Encephalocraniocutaneous lipomatosis: report of two cases P0692 Dyskeratosis congenita: a familial form P0693 Dyschromatosis symmetric hereditaria: analyses of clinical and genetic features P0694 Acrokeratotic poikiloderma (PED type XII) the additional case report and review the literature P0695 Aarau disease P0696 Accessory tragus and its importance for dermatology P0697 Eruptive dermatitis in treated maple syrup urine disease (MSUD) P0698 Cutaneous findings in Rubinstein-Taybi syndrom P0699 Keratolytic winter erythema P0700 Hidrotic ectodermal dysplasia. A tunisian family group case P0701 Xeroderma pigmentosum in Yemen P0702 Mutation analysis of the pten gene in japanese cases of Cowden disease P0703 A mother and her son: intrafamilial phenotype variation of neurofibromas seen in NF1 patients P0704 Pachyonychia congenita: cases report P0705 A mutation in connexin 31 is associated with recessive erythrokeratodermia variabilis (EKV) and leads to defective membranous localization P0706 Focal dermal hypoplasia syndrome: report of ten patients, three of them were males P0707 Localized scleroderma in childhood: a report of 28 cases P0708 Neurofibromatosis presenting as peripheral nerve thickening P0709 Bloom syndrome (study of 8 cases) P0710 Effective bleomycin local injection therapy in multiple cutaneous tumor of von Recklinghausen disease P0711 A particular form of photogenodermatosis: report of 2 cases in siblings P0712 The kindler and weary syndromes. A clinical case P0713 Fabry's disease and hypoparathyroidism P0714 Squamous cell carcinoma complicating an hereditary epidermolysis bullosa P0715 Congenital giant cell pigmented nevus, giant hairy nevus and hemangioma P0716 Porokeratosis of Mibelli with giant lesions P0717 Darier's disease, experience of 15 years at the General Hospital of Mexico P0718 Nevoid hyperkeratosis of the areolae in a 14-year-old filipino female P0719 Fabry's disease P0720 Pseudoxanthoma elasticum. Report of six patients P0721 Pili torti et canaliculi and agenesis of teeth. A new hair-teeth ectodermal dysplasia P0722 A case of congenital erythropoietic porphyria P0723 Mal De Meleda - syndrome keratoderma palmoplantaris transgredien's P0724 Pibids syndrome and spinocellular carcinoma of the face P0725 Mosaic epidermolytic hyperkeratosis P0726 Atopic dermatitis in pediatric patients with monogenic genetic defects P0727 Course of hereditary dermatoses during pregnancy P0728 Erythrokeratoderma variabilis in a father and daughter P0729 Cockayne disease: report of three families P0730 Rothmund-Thomson syndrome P0731 Lichen striatus with multiple lesions fallowing the lines of Blaschko P0732 Prevalence of Epidermolysis Bullosa Hereditaria in Bulgaria P0733 A particular case of xeroderma pigmentosum with internal malignancy P0734 Xeroderma pigmentosum patient with multiple melanomas P0735 Routine autoradiographic analysis of DNA excision-repair. Report of prenatal diagnosis in 7 tunisian families P0736 Detection of gene mutation in a Chinese pedigree with X-linked anhidrotic ectodermal dysplasia (EDA) by PCR-SSCP analysis P0737 Cutis verticis gyrata: two brothers cases					1st TO 5th JULY 2002 PARIS Back to main menu Foreword Oral communications and co-opted speakers abstracts Poster abstracts Searching by Author's name Searching by Article's number

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