The report of two cases with multiple sulfatase deficiency resulting from a rare similar gene mutation.

Ashrafzadeh, Farah; Zabolinejad, Naghmeh; Ghayoor Karimiani, Ehsan; Beiraghi Toosi, Mehran; Doniadideh, Nahid; Torabi, Shatila; Razmyar, Mohammad; Sheikh Andalibi, Mohammad S

Ashrafzadeh, Farah; Zabolinejad, Naghmeh; Ghayoor Karimiani, Ehsan; Beiraghi Toosi, Mehran; Doniadideh, Nahid; Torabi, Shatila; Razmyar, Mohammad; Sheikh Andalibi, Mohammad S.

Affiliation

Ashrafzadeh F; Department of Pediatric Neurology, Mashhad University of Medical Sciences, Mashhad, Iran.
Zabolinejad N; Cutaneous Leishmaniasis Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Ghayoor Karimiani E; Razavi Cancer Research Center, Razavi Hospital, Imam Reza international university, Mashhad, Iran.
Beiraghi Toosi M; Department of Pediatric Neurology, Mashhad University of Medical Sciences, Mashhad, Iran.
Doniadideh N; Department of Pediatrics, Mashhad University of Medical Sciences, Mashhad, Iran.
Torabi S; Cutaneous Leishmaniasis Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Razmyar M; Cutaneous Leishmaniasis Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Sheikh Andalibi MS; Student Research Committee, Cardiovascular Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Int J Dermatol ; 57(10): 1242-1245, 2018 10.

Article de En | MEDLINE | ID: mdl-29479672

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Sulfuric ester hydrolases / Déficit multiple en sulfatases Type d'étude: Etiology_studies Limites: Child, preschool / Female / Humans / Infant / Male Langue: En Journal: Int J Dermatol Année: 2018 Type de document: Article Pays d'affiliation: Iran

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