Diamond-Blackfan anemia natural history, complications and prognosis: Difference between revisions

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==Overview==
==Overview==
If left untreated, [#]% of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].
OR
Common complications of [disease name] include [complication 1], [complication 2], and [complication 3].
OR
Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately
==Diamond-Blackfan anemia natural history, complications and prognosis==
==Diamond-Blackfan anemia natural history, complications and prognosis==
'''Natural history'''
'''Natural history'''

Revision as of 22:24, 7 August 2020

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Overview

If left untreated, [#]% of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].

OR

Common complications of [disease name] include [complication 1], [complication 2], and [complication 3].

OR

Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately

Diamond-Blackfan anemia natural history, complications and prognosis

Natural history The severity of Diamond-Blackfan anemia may vary, even within the same family.

  • Classic DBA:
    • Symptoms of anemia include fatigue, weakness, and an abnormally pale appearance (pallor).
    • The symptomatic onset of Diamond black-fan anemia becomes apparent during the first year of life
  • Approximately half of DBA cases have Congenital malformations, in particular craniofacial, upper-limb, heart, and genitourinary malformations:(observed in ~30%-50%):
  • All diagnostic criteria are met.
  • Non-classic DBA:
    • presents with mild or absent anemia with only subtle indications of erythroid abnormalities such as macrocytosis, elevated ADA, and/or elevated HbF concentration
    • Have mild anemia beginning later in childhood or in adulthood, while others have some of the physical features but no bone marrow problems.
    • Minimal or no evidence of congenital anomalies or short stature[1]

References

  1. Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean L, Stephens K, Amemiya A, Clinton C, Gazda HT. PMID 20301769. Vancouver style error: initials (help); Missing or empty |title= (help)