Cargando…
Pulmonary hypertension and vasculopathy in incontinentia pigmenti: a case report
Incontinentia pigmenti (IP; Bloch–Sulzberger syndrome) is a rare, genetic syndrome inherited as an X-linked dominant trait. It primarily affects female infants and is lethal in the majority of males during fetal life. The clinical findings include skin lesions, developmental defects, and defects of...
Autores principales: | Alshenqiti, Abduljabbar, Nashabat, Marwan, AlGhoraibi, Hissah, Tamimi, Omar, Alfadhel, Majid |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431708/ https://www.ncbi.nlm.nih.gov/pubmed/28533687 http://dx.doi.org/10.2147/TCRM.S134705 |
Ejemplares similares
-
Incontinentia pigmenti
por: Poziomczyk, Cláudia Schermann, et al.
Publicado: (2014) -
Case Reports of Incontinentia Pigmenti in Males
por: Gupta, Khushboo D, et al.
Publicado: (2013) -
Retinopathy in incontinentia pigmenti
por: Rishi, Pukhraj, et al.
Publicado: (2019) -
A case of reversible pulmonary arterial hypertension associated with
incontinentia pigmenti
por: Atallah, Veronique, et al.
Publicado: (2018) -
Retinal imaging in incontinentia pigmenti
por: Narang, Subina, et al.
Publicado: (2019)