Unusual presentation: Pulmonary hemosiderosis with celiac disease and retinitis pigmentosa in a child | Zendy

Keskin Ozlem | Zendy; Keskin Mehmet | Zendy; Guler Elif | Zendy; Tutar Ediz | Zendy; Saygili Oguzhan | Zendy; Kucukosmanoglu Ercan | Zendy; Kor Yilmaz | Zendy; Celik Haydar | Zendy; Coskun Enes | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Unusual presentation: Pulmonary hemosiderosis with celiac disease and retinitis pigmentosa in a child

Author(s) -

Keskin Ozlem,

Keskin Mehmet,

Guler Elif,

Tutar Ediz,

Saygili Oguzhan,

Kucukosmanoglu Ercan,

Kor Yilmaz,

Celik Haydar,

Coskun Enes

Publication year - 2011

Publication title -

pediatric pulmonology

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.866

H-Index - 106

eISSN - 1099-0496

pISSN - 8755-6863

DOI - 10.1002/ppul.21420

Subject(s) - hemosiderosis , medicine , presentation (obstetrics) , retinitis pigmentosa , disease , pediatrics , rare disease , anemia , case presentation , pathology , surgery , retinal , ophthalmology

Idiopathic pulmonary hemosiderosis (IPH) is a rare disease characterized by anemia, hemoptysis and recurrent alveolar hemorrhage. The combination of IPH and celiac disease (CD) is extremely rare. We report a 9‐year‐old boy with Lane‐Hamilton syndrome, co‐occurrence of pulmonary hemosiderosis with CD. This presentation is unique presentation because he has also retinal pigmentation. Pediatr. Pulmonol. 2011; 46:820–823. © 2011 Wiley‐Liss, Inc.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research