diseases

Wiskott Aldrich Syndrome

Wiskott-Aldrich syndrome is a rare genetic immunodeficiency that keeps a child's immune system from functioning properly. It also makes it difficult for a child's bone marrow to produce platelets, making a child prone to bleeding. It occurs mostly in males.

Posted September 23, 2022 by Anusha ‐ 3 min read

⌖ diseases treatments syndromes disorders wiskott-aldrich-syndrome aldrich-syndrome health

Kostmann's Syndrome

Posted September 23, 2022 by Anusha ‐ 2 min read

⌖ diseases treatments syndromes disorders severe-congenital-neutropenia scn infantile-genetic-agranulocytosis health

LADD Syndrome

Lacrimo-auriculo-dento-digital (LADD) syndrome is an extremely rare genetic disorder characterized by abnormalities affecting the lacrimal and salivary glands and ducts, ears, teeth and fingers and toes.

Posted September 23, 2022 by Anusha ‐ 3 min read

⌖ diseases treatments syndromes lacrimo-auriculo-dento-digital-syndrome disorders health levy-hollister-syndrome ladd-syndrome

Papillon Lefevre Syndrome

Papillon-Lefèvre syndrome (PLS) is an extremely rare genetic disorder that typically becomes apparent from approximately one to five years of age. PLS is characterized by the development of dry scaly patches on the skin of the palms and the soles.

Posted September 23, 2022 by Anusha ‐ 3 min read

⌖ diseases treatments syndromes disorders health papillon-lefevre-syndrome

Kallmann Syndrome

Kallmann syndrome is a condition that’s characterized by absent or delayed puberty and a lack or loss of sense of smell. Kallmann syndrome may be accompanied by other symptoms, including hearing loss and cleft palate. The condition is typically treated with hormone replacement therapy.

Posted September 23, 2022 by Anusha ‐ 2 min read

⌖ diseases treatments syndromes disorders health kallmann-syndrome