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1983 1
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Page 1
Genetically induced abnormalities of epidermal differentiation and ultrastructure in ichthyoses and epidermolyses: pathogenesis, heterogeneity, fetal manifestation, and prenatal diagnosis.
Anton-Lamprecht I. Anton-Lamprecht I. J Invest Dermatol. 1983 Jul;81(1 Suppl):149s-56s. doi: 10.1111/1523-1747.ep12540961. J Invest Dermatol. 1983. PMID: 6345689 Free article. Review.
Expression of mutant genes during fetal life and fetal manifestation of such abnormalities are a precondition for the prenatal diagnosis of genetic skin disorders (bullous ichthyosiform erythroderma, epidermolysis bullosa dystrophica Hallopeau-Siemens, Herlit …
Expression of mutant genes during fetal life and fetal manifestation of such abnormalities are a precondition for the prenatal diagnosis of …
Clinico-epidemiological features of primary hereditary ichthyoses in the Eastern province of Saudi Arabia.
Al-Zayir AA, Al-Amro Al-Alakloby OM. Al-Zayir AA, et al. Int J Dermatol. 2006 Mar;45(3):257-64. doi: 10.1111/j.1365-4632.2006.02042.x. Int J Dermatol. 2006. PMID: 16533225
Thirty-one patients (44.7%) with Ichthyosis Vulgaris (IV) were seen: 12 patients (16.9%) with X-linked Recessive Ichthyosis (XLRI), four patients (5.6%) with Lamellar Ichthyosis (LI), three patients (4.2%) with Bullous Ichthyosiform Erythroderma (BIE) and 21 …
Thirty-one patients (44.7%) with Ichthyosis Vulgaris (IV) were seen: 12 patients (16.9%) with X-linked Recessive Ichthyosis (XLRI), four pat …
Clinical investigation of acitretin in children with severe inherited keratinization disorders in China.
Zhang XB, Luo Q, Li CX, He YQ, Xu X. Zhang XB, et al. J Dermatolog Treat. 2008;19(4):221-8. doi: 10.1080/09546630801955150. J Dermatolog Treat. 2008. PMID: 18608715 Clinical Trial.
RESULTS: After 2-4 months of treatment, the clinical cure rate was 82.1% and the effective rate was 17.9%. Most cases, such as bullous ichthyosiform erythroderma, lamellar ichthyosis, pityriasis rubra pilaris, and inflammatory linear verrucous epidermal nevus …
RESULTS: After 2-4 months of treatment, the clinical cure rate was 82.1% and the effective rate was 17.9%. Most cases, such as bullous …
Primary hereditary ichthyoses in the Eastern Province of Saudi Arabia.
Al-Zayir AA, Al-Amro Alakloby OM. Al-Zayir AA, et al. Int J Dermatol. 2004 Jun;43(6):415-9. doi: 10.1111/j.1365-4632.2004.01687.x. Int J Dermatol. 2004. PMID: 15186221
The clinical pattern of PHI was as follows: 31 patients (44.7%) with ichthyosis vulgaris (IV), 12 (16.9%) with X-linked recessive ichthyosis (XLRI), four (5.6%) with lamellar ichthyosis (LI), three (4.2%) with bullous ichthyosiform erythroderma (BIE), and 21 …
The clinical pattern of PHI was as follows: 31 patients (44.7%) with ichthyosis vulgaris (IV), 12 (16.9%) with X-linked recessive ichthyosis …
An appraisal of acitretin therapy in children with inherited disorders of keratinization.
Lacour M, Mehta-Nikhar B, Atherton DJ, Harper JI. Lacour M, et al. Br J Dermatol. 1996 Jun;134(6):1023-9. Br J Dermatol. 1996. PMID: 8763418 Clinical Trial.
Forty-six children have received acitretin since 1992 in our hospital: 29 children had either lamellar ichthyosis (nine), non-bullous ichthyosiform erythroderma (five), bullous ichthyosiform erythroderma (four), Sjogren-Larsson syndrome ( …
Forty-six children have received acitretin since 1992 in our hospital: 29 children had either lamellar ichthyosis (nine), non-bullous …
The clinical spectrum of congenital ichthyosis in Sweden: a review of 127 cases.
Vahlquist A, Gånemo A, Pigg M, Virtanen M, Westermark P. Vahlquist A, et al. Acta Derm Venereol Suppl (Stockh). 2003 May;(213):34-47. Acta Derm Venereol Suppl (Stockh). 2003. PMID: 12822194
Applying a combination of phenotypic and genotypic criteria, the patients were classified into three main groups: 1) Bullous ichthyosis (epidermolytic hyperkeratosis) and related disorders due to keratin mutations (n = 21); 2) Non-bullous ichthyosiform erythroder …
Applying a combination of phenotypic and genotypic criteria, the patients were classified into three main groups: 1) Bullous ichthyosis (epi …
Ichthyosiform erythroderma associated with generalized pustulosis.
Langtry JA, Carr MM, Ive FA, Gordon P, Hunter JA, Harper JI. Langtry JA, et al. Br J Dermatol. 1998 Mar;138(3):502-5. doi: 10.1046/j.1365-2133.1998.02133.x. Br J Dermatol. 1998. PMID: 9580808
Two unrelated boys are described who were born as collodion babies and subsequently developed non-bullous ichthyosiform erythroderma and flares of generalized sterile pustulosis, similar to generalized pustular psoriasis. ...
Two unrelated boys are described who were born as collodion babies and subsequently developed non-bullous ichthyosiform ery …
Harlequin baby: a case report.
Singalavanija S, Sangtawesin V, Horpoapan S, Ratrisawadi V. Singalavanija S, et al. J Med Assoc Thai. 1998 May;81(5):365-70. J Med Assoc Thai. 1998. PMID: 9623037
Now she is over three years old and the skin developed into congenital non-bullous ichthyosiform erythroderma. Unfortunately she had delayed growth and development. ...
Now she is over three years old and the skin developed into congenital non-bullous ichthyosiform erythroderma. Unfortun …
"Blind" versus direct vision technique for fetal skin sampling in cases for prenatal diagnosis.
Löfberg L, Gustavii B. Löfberg L, et al. Clin Genet. 1984 Jan;25(1):37-41. doi: 10.1111/j.1399-0004.1984.tb00460.x. Clin Genet. 1984. PMID: 6368057
Seven fetuses at risk of developing a serious inherited skin disorder (epidermolysis bullosa atrophicans generalisata gravis in 4, bullous ichthyosiform erythroderma in 2, and non-bullous ichthyosiform erythroderma in 1) were subjected to …
Seven fetuses at risk of developing a serious inherited skin disorder (epidermolysis bullosa atrophicans generalisata gravis in 4, bullou …