Agenesis of corpus callosum, severe developmental delay, recurrent infections, and cutaneous hypopigmentation: a case of Vici syndrome

Autor: Fatima Rauf, Sidra Rauf, Mansoor-ul-Haq Mansoor-ul-Haq

Publikováno v: European Journal of Medical Case Reports. :226-229

Background: Vici syndrome is a rare, autosomal recessive multisystem disorder, first described in 1988 by Dionisi-Vici. This syndrome is characterized by corpus callosum agenesis, oculocutaneous hypopigmentation, cataracts, immunodeficiency, and card

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2c5e1b7b0f38ba29864c66bd41a24c16
https://doi.org/10.24911/ejmcr/173-1605461194

Impact Of Patient, Disease and Plasma Exchange Characteristics On The Outcomes Of Thrombotic Thrombocytopenic Purpura In a Retrospective Cohort Study

Autor: Khattak, Amna G ^*, Haq, Mansoor Ul, Kaweeta, Fnu ^*, Kocak, Mehmet ^*, Bradley, Robert ^*, Weir, Alva B.

Publikováno v: In Blood 15 November 2013 122(21):2359-2359

Aortoenteric fistula - A fatal cause of gastrointestinal bleeding. Can it be missed? - A case report.

Autor: Ahmad BS; Liaquat National Hospital., Haq MU; Liaquat National Hospital., Munir A; Ziauddin University, Karachi., Abubakar Mohsin Ehsanullah SA; Ziauddin University, Karachi., Ashraf P; Liaquat National Hospital.

Publikováno v: JPMA. The Journal of the Pakistan Medical Association [J Pak Med Assoc] 2018 Oct; Vol. 68 (10), pp. 1535-1537.