Results 21 to 30 of about 1,259,329 (163)
A Case Report of Incontinentia Pigmenti in a Newborn with Positive Family History Extending Over Three Generations [PDF]
Iranian Journal of Neonatology, 2017 Background: Incontinentia pigmenti (IP), also known as Bloch-Sulzberger syndrome, is a rare X-linked dominant genodermatosis that presents at the time of birth or soon after birth with cutaneous manifestation. This disorder may also affect the ectodermal
Seyedeh Fatemeh Khatami +4 more
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Síndrome de Bloch-Sulzberger – uma genodermatose rara: relato de caso [PDF]
, 2021 Objetivos: Considerando que a Síndrome de Bloch-Sulzberger é uma genodermatose rara e que apresenta importantes manifestações na cavidade bucal, o presente estudo teve como objetivos relatar um caso de uma lactente e enfatizar a importância da abordagem ...
Santos, Leticia Oliveira dos
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A case of reversible pulmonary arterial hypertension associated with incontinentia pigmenti
Pulmonary Circulation, Volume 8, Issue 4, Page 1-3, October-December 2018., 2018 Incontinentia pigmenti (IP) is a multisystemic disorder in which pulmonary arterial hypertension (PAH) is a severe and rarely reported association. The prognosis has been poor in reported cases. In our patient, IP was diagnosed during the neonatal period with a combination of cutaneous, ophthalmic, and neurological symptoms.
Veronique Atallah +7 more
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Incontinentia pigmenti with neurologic and oculodental disorders
Indian Journal of Paediatric Dermatology, 2016 Incontinentia pigmenti is a genodermatosis with X-linked dominant inheritance, characterized by cutaneous, neurologic, ophthalmologic, and dental abnormalities with a pattern suggestive of somatic mosaicism.
Jorge Arturo Avina Fierro +1 more
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Incontinentia Pigmenti Misdiagnosed as Neonatal Herpes Simplex Virus Infection
Case Reports in Pediatrics, Volume 2018, Issue 1, 2018., 2018 Incontinentia pigmenti (IP) is an X‐linked dominant neurocutaneous syndrome with ophthalmologic, neurologic, cutaneous, and dental manifestations and in most cases antenatally lethal in boys. Occasionally, typical IP may occur in boys due to Klinefelter syndrome or a genomic mosaicism. Skin lesions are observed in 4 stages: blistering, verrucous linear
Fahimeh Abdollahimajd +6 more
wiley +1 more source
The frequency of intraocular hemorrhage in hereditary vitreoretinal dystrophies
Российский офтальмологический журнал, 2018 Hereditary vitreoretinal degenerations are a heterogeneous group of diseases, which are based on the degenerative changes of the retina and the vitreous. The occurrence of intrahemorrhages is different for different hereditary vitreoretinal degenerations.
O. Yu. Yatsenko, O. S. Velibekova
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Talon Cusp Type I: Restorative Management
Case Reports in Dentistry, Volume 2015, Issue 1, 2015., 2015 The teeth are formed during intrauterine life (i.e., gestation) during the odontogenesis stage. During this period, the teeth move until they enter the oral cavity. This course covers various stages of dental development, namely, initiation, proliferation, histodifferentiation, morphodifferentiation, and apposition.
Rafael Alberto dos Santos Maia +4 more
wiley +1 more source
Congenital and Acquired Abnormalities of the Corpus Callosum: A Pictorial Essay
BioMed Research International, Volume 2013, Issue 1, 2013., 2013 The purpose of this review is to illustrate the wide spectrum of lesions in the corpus callosum, both congenital and acquired: developmental abnormalities, phakomatoses, neurometabolic disorders, demyelinating diseases, infection and inflammation, vascular lesions, neoplasms, traumatic and iatrogenic injury, and others. Cases include fetuses, children,
Katarzyna Krupa +2 more
wiley +1 more source
Incontinentia pigmenti: case report and 5-year follow-up
Acta Odontologica Turcica, 2017 Introduction: Incontinentia Pigmenti (Bloch-Sulzberger Syndrome) is a disease of organ involvement with ectodermic and mesodermic origin, showing dominant transition based on the X-chromosome. It affects the skin, eyes, teeth, and central nervous system.
Ayşegül Sarı, Salih Çelik
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Bloch Sulzberger syndrome (Incontinentia pigmenti): A rare case report with dental defects
Journal of Indian Society of Pedodontics and Preventive Dentistry, 2015 Incontinentia Pigmenti (IP) is a multisystem genodermatosis characterized by cutaneous, neurologic, ophthalmologic, and dental abnormalities. This article reports the clinical features and management of a 4-year-old girl diagnosed with IP.
Yaga Uday Shankar +3 more
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