The 20 Best Henoch-Schonlein Purpura Doctors Near Me in Gharb-Chrarda-Beni Hssen, MA

Find the Top Henoch-Schonlein Purpura Experts and Specialists

Last Updated: 04/28/2026

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MediFind found 5 doctor with experience in Henoch-Schonlein Purpura near Gharb-Chrarda-Beni Hssen, MA. Of these, 5 are Experienced.

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5 providers found
    Experienced in Henoch-Schonlein Purpura

    Aziza Elouali
    Experienced in Henoch-Schonlein Purpura

    Aziza Elouali
    Oujda-angad, MA 

    Aziza Elouali practices practicing medicine in Oujda-angad, Morocco. Ms. Elouali is rated as an Experienced expert by MediFind in the treatment of Henoch-Schonlein Purpura. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Enlarged Liver, Pycnodysostosis, Leukocytosis, Bone Marrow Aspiration, and Fasciotomy.

    Experienced in Henoch-Schonlein Purpura

    Abdeladim Babakhouya
    Experienced in Henoch-Schonlein Purpura

    Abdeladim Babakhouya
    Oujda-angad, MA 

    Abdeladim Babakhouya practices practicing medicine in Oujda-angad, Morocco. Babakhouya is rated as an Experienced expert by MediFind in the treatment of Henoch-Schonlein Purpura. They are also highly rated in 4 other conditions, according to our data. Their clinical expertise encompasses Enlarged Liver, Leukocytosis, Kawasaki Disease, Bone Marrow Aspiration, and Fasciotomy.

    Experienced in Henoch-Schonlein Purpura

    Maria Rkain
    Experienced in Henoch-Schonlein Purpura

    Maria Rkain
    Oujda-angad, MA 

    Maria Rkain practices practicing medicine in Oujda-angad, Morocco. Ms. Rkain is rated as an Experienced expert by MediFind in the treatment of Henoch-Schonlein Purpura. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses Enlarged Liver, Leukocytosis, Chickenpox, Bone Marrow Aspiration, and Fasciotomy.

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    Experienced in Henoch-Schonlein Purpura

    Chaimae N'joumi
    Experienced in Henoch-Schonlein Purpura

    Chaimae N'joumi
    Oujda-angad, MA 

    Chaimae N'joumi practices practicing medicine in Oujda-angad, Morocco. N'joumi is rated as an Experienced expert by MediFind in the treatment of Henoch-Schonlein Purpura. Their clinical expertise encompasses Brachydactyly, Piebaldism, Klippel-Trenaunay Syndrome, Chediak-Higashi Syndrome, and Fasciotomy.

    Experienced in Henoch-Schonlein Purpura

    Mohamed Belahcen
    Experienced in Henoch-Schonlein Purpura

    Mohamed Belahcen
    Oujda-angad, MA 

    Mohamed Belahcen practices practicing medicine in Oujda-angad, Morocco. Mr. Belahcen is rated as an Experienced expert by MediFind in the treatment of Henoch-Schonlein Purpura. His clinical expertise encompasses Hygroma Cervical, Cystic Hygroma, Cavernous Lymphangioma, Chondroma, and Fasciotomy.

    While we make every effort to provide the best results possible, data is currently limited outside of the United States. Doctors listed may include both clinicians and researchers, and individuals relocate frequently. We recommend contacting doctors directly to confirm their location and areas of focus. Contact information is provided when available. Learn more about our expert tiers.
    Showing 1-5 of 5

    Last Updated: 04/28/2026

    What is the definition of Henoch-Schonlein Purpura?

    Henoch-Schonlein purpura (HSP), also called immunoglobulin A vasculitis (IgAV), is a vascular disease that primarily affects small blood vessels. The disease is characterized by abnormal deposits of immunoglobulin A (an antibody) in the blood vessels, leading to their inflammation (vasculitis). The small vessels of the skin, joints, kidneys, and digestive organs are particularly involved. Signs and symptoms usually begin suddenly (and progress over days) and may include purple-colored spots on the skin (purpura); joint pain; and gastrointestinal problems such as abdominal pain, nausea, bloody stools, and rarely, severe complications requiring surgery. People with HSP may also develop glomerulonephritis (injury to the kidneys caused by inflammation) and poor kidney function, which may result in swelling of parts of the body or face (edema), and blood and protein in the urine (hematuria and proteinuria). Most cases of HSP occur in children and go away without causing serious or long-term health problems. Less commonly, the disease affects adults and may be more severe, leading to chronic kidney disease and kidney failure. The cause of HSP is not completely understood, but research indicates that genes (especially those involved in regulating the immune system) may play a key role in predisposing a person to HSP, as well as its severity. However, while genes may increase the risk of developing the disease (and in some cases more than one family member has HSP), the disease itself is not inherited. The diagnosis of HSP may be made based on symptoms, blood and urine tests, imaging studies, and/or a biopsy of the skin or kidney.