[Hemoglobin SD disease]

Monatsschr Kinderheilkd. 1993 Sep;141(9):708-10.
[Article in German]

Abstract

A 7 year old Kurdish girl presented with a cerebral infarction and a resulting hemiparesis following a blood transfusion. Examination of the blood film suggested sickle cell anaemia. However a simultaneously carried out haemoglobin electrophoresis showed haemoglobin S and haemoglobin D. The diagnosis of haemoglobin SD disease was thereby established. This kind of haemoglobin disorder usually shows a mild clinical manifestation. According to our knowledge such serious cases have not been published before. With this disease the main emphasis is on the prevention of recurrent cerebral infarctions bay a long-term transfusion programme whereas the effects of the cerebral infarction are treated in the usual way.

Publication types

  • Case Reports

MeSH terms

  • Anemia, Sickle Cell / diagnosis
  • Anemia, Sickle Cell / genetics
  • Brain / pathology
  • Cerebral Infarction / diagnosis
  • Cerebral Infarction / genetics
  • Child
  • Diagnosis, Differential
  • Female
  • Genetic Carrier Screening*
  • Hemoglobin SC Disease / diagnosis
  • Hemoglobin SC Disease / genetics*
  • Hemoglobin, Sickle / genetics*
  • Hemoglobins, Abnormal / genetics*
  • Humans
  • Magnetic Resonance Imaging
  • Thalassemia / diagnosis
  • Thalassemia / genetics*

Substances

  • Hemoglobin, Sickle
  • Hemoglobins, Abnormal
  • hemoglobin D Punjab
  • hemoglobin Arab