Bloch — Sulzberger syndrome [PDF]
Саратовский научно-медицинский журнал, 2015 Five clinical observations in pediatric patients with Bloch — Sulzberger syndrome are presented. The observation had been performed for six months. The differential diagnosis depending on the stage of the disease was done.
Slesarenko N.A. +4 more
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Incontinentia pigmenti or Bloch-Sulzberger syndrome: a rare X-linked genodermatosis [PDF]
Anais Brasileiros de Dermatologia, 2014 Incontinentia pigmenti is a rare X-linked genodermatosis that affects mainly female neonates. The first manifestation occurs in the early neonatal period and progresses through four stages: vesicular, verruciform, hyperpigmented and hypopigmented ...
Gabriela Franco Marques +2 more
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Magnetic resonance imaging for diagnosing a rare disease: incontinentia pigmenti (Bloch–Sulzberger syndrome) on the example of a clinical case [PDF]
Digital Diagnostics, 2023 Incontinentia pigmenti, also known as Bloch–Sulzberger syndrome, is a rare hereditary disease characterized by typical skin rashes and involvement of other organs and systems.
Igor I. Yarmola +8 more
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Incontinentia pigmenti (Bloch-Sulzberger syndrome). [PDF]
Journal of Medical Genetics, 1993 D Donnai
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Oral Rehabilitation as Part of a Multidisciplinary Treatment in a Case Study of Pigmentary Incontinence [PDF]
Children, 2023 We present the clinical course of a 9-year-old female patient with Bloch–Sulzberger syndrome and severe neurological deficit that met the major (classic cutaneous signs) and minor (dental anomalies and retinal pathology) diagnostic criteria of Landy and ...
Mónica Cano-Rosás +6 more
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Incontinentia Pigmenti: A Case Report of Early Clinical Symptoms in a Lack of Family Inheritance Positive Result [PDF]
Clinical, Cosmetic and Investigational Dermatology, 2023 Fang Yuan,1,* Feng-Na Zhu,2,* Xiao-Juan Liu,1,* Jun Li,3 Hong-Tao Xu1 1Department of Pediatrics, General Hospital of Central Theater Command of the People’s Liberation Army, Wuhan, 430070, People’s Republic of China; 2Department of ...
Yuan F, Zhu FN, Liu XJ, Li J, Xu HT
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Clinical case of Bloch — Sulzberger syndrome
Vestnik Dermatologii i Venerologii, 2020 Purpose.To present a clinical case of Bloch Sulzberger syndrome. Material and methods. The examinations were performed to diagnose the disease: а visual examination of the skin, cytological analysis of the gallbladder fluid, general and biochemical ...
Nadezhda V. Krasnova +5 more
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Case report: Variability in clinical manifestations within a family with incontinentia pigmenti [PDF]
Frontiers in MedicineDiagnosing skin diseases in children can be a complex interdisciplinary problem. Incontinentia pigmenti (IP), also known as Bloch-Sulzberger syndrome, is a rare hereditary genodermatosis related to a mutation in the IKBKG gene.
Tatiana Belysheva +18 more
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Dental treatment considerations for a pediatric patient with incontinentia pigmenti (Bloch-Sulzberger syndrome) [PDF]
European Journal of Dentistry, 2017 Chen AY, Chen K.
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BLOCH-SULZBERGER SYNDROME (CLINICAL CASE)
Мать и дитя в КузбассеBloch-Sulzberger syndrome is a rare genodermatosis or pigment incontinence syndrome found in the first weeks of life. The syndrome belongs to the group of systemic melanoblastoses. Its frequency is 1 in 10000 girls or 1 in 75000 newborns.
Светлана Ивановна Елгина +9 more
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