Results 31 to 40 of about 1,259,329 (163)
Bloch-Sulzberger syndrome: a description of the clinical case [PDF]
, 2020 The article describes the clinical case of Bloch-Sulzberger syndrome, a rare genodermatosis, characterized by specific phasic changes in the skin and appendages of skin in conjunction with pathologies of nervous, locomotor and visual systems.
Zakharov, M. A. +5 more
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Anais Brasileiros de Dermatologia, 2010 A incontinência pigmentar é uma genodermatose rara, ligada ao X, que afeta, principalmente, neonatos do sexo feminino. As manifestações cutâneas são as mais prevalentes, e ocorrem em quatro fases bem distintas. Lactente feminina com lesões vesicobolhosas
Marcela A. C. Pereira +4 more
doaj +1 more source
, 2000 Incontinentia Pigmenti (Bloch-Sulzberger syndrome) is a rare multisystem, ectodermal disorder associated with dermatological, dental and ocular features, and ...
Pal, K +7 more
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Incontinentia pigmenti presenting as hypodontia in a 3-year-old girl: a case report
Journal of Medical Case Reports, 2009 Introduction Incontinentia pigmenti or Bloch-Sulzberger syndrome is a rare X-linked dominant disease that mainly affects the skin, eyes, hair, central nervous system and teeth. The disease is predominant among women.
Kitakawa Dárcio +4 more
doaj +1 more source
Familial recurrence of incontinentia pigmenti due to de novo pathogenic variants in the IKBKG gene
American Journal of Medical Genetics Part A, Volume 194, Issue 8, August 2024.Abstract Incontinentia pigmenti (IP, Bloch‐Sulzberger syndrome) is a multisystem disorder which associates specific skin lesions that evolves in four stages, and occasionally, central nervous system, eye, hair, and teeth involvement. Familial (35%) and sporadic (65%) cases are caused by pathogenic variants in the IKBKG gene.
Julie Steffann +5 more
wiley +1 more source
Incontinentia pigmenti in a child with suspected retinoblastoma
International Journal of Retina and Vitreous, 2017 Background Incontinentia pigmenti is a rare X-linked dominant syndrome caused by mutation in the NEMO/IKKgamma gene, and characterized by a spectrum of cutaneous, ocular, neurologic and dental abnormalities.
Stephanie J. Weiss +3 more
doaj +1 more source
Syndrome of Bloch-Sulzberger. [PDF]
, 2019 The article presents literature data on the etiology and pathogenesis, clinical and laboratory diagnosis of rare dermatosis - Bloch-Sulzberger syndrome.
Сорокина, К. Н. +3 more
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Broodstock management and seed production of the rabbitfish Siganus guttatus (Bloch) and the sea bass Lates calcarifer (Bloch) [PDF]
, 1988 This paper reviews results of studies conducted on the rabbitfish, Siganus guttatus (Bloch) and the sea bass Lates calcarifer (Bloch) at the Aquaculture Department of the Southeast Asian Fisheries Development Center.
Duray, Marietta N., Juario, Jesus V.
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Vestnik dermatologii i venerologii, 2012 The author describes a rare case of dermatosis in children — incontinentia pigmenti. The author also describes manifestations characteristic of the Bloch — Sulzberger syndrome. All stages of the disease are presented in detail.
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Bloch–Sulzberger syndrome (Incontinentia pigmenti)
Russian Journal of Skin and Venereal Diseases, 2023 Bloch–Sulzberger syndrome or Incontinentia pigmenti is a genetic disease that causes skin pathology in the first days of a child's life and is suspected of identifying the disease. The article presents the characteristic signs of this syndrome and the pronounced manifestations of the disease.
Svetlana N. Shchava, Marina A. Shishkina
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