Question 15 (part 2) · LEK · Wiskott-Aldrich syndrome
The typical features for the recognition of Wiskott-Aldrich syndrome are:
- A. girl, recurrent skin abscesses, impaired neutrophil function.
- B. facial dysmorphia, weight and height deficiency, IgG subclass deficiency.
- C. boy, thrombocytopenia, atopic dermatitis, persistent infections.
- D. facial dysmorphia, congenital heart disease, tetany, absence or hypoplasia of the thymus gland.
- E. mental retardation, thrombocytopenia, megaloblastic anemia.
Hint
This X-linked disorder has a classic triad affecting platelets, skin and immunity.
The answer, the explanation and a note on every option are available once you log in. The account is free: topic tests, a mock exam, mistake review and statistics.
More questions on Pediatrics
- An increased pulmonary flow in congenital heart defects with the left-right leakage leads to structural changes in the pulmonary arterioles, which…
- If the incidental glucose concentration is 14 mmol / L and pollakiuria and polyuria occur, then to confirm the diagnosis of type I diabetes mellitus…
- A 13-year-old girl reported to the pediatrician with the following history: decreased concentration, deterioration of learning performance, hair…
- In haemophilia B, the deficiency relates to the factor:
- In the course of B19 parvovirus infection, the development of the following may occur.
- The Apgar scoring includes an assessment of the following features except for: