-transparent.png){kind=logo}
The manifestations of the sickling disorders are becoming increasingly familiar to clinicians in Great Britain. One of these disorders, sickle-cell haemoglobin disease, has hitherto received little attention, being regarded as a relatively mild condition. This paper describes some of the distinctive clinical features of the disease as seen in a series of nine cases which have recently presented in London, two of which were fatal. The special hazards of the condition in relation to pregnancy, air travel, and general anaesthesia are discussed.
Related Publications
A J Black, and
P I Condon, and
B M Gompels, and
R L Green, and
R G Huntsman, and
G C Jenkins
June 1958,
The West African medical journal,
A J Black, and
P I Condon, and
B M Gompels, and
R L Green, and
R G Huntsman, and
G C Jenkins
March 1969,
British medical journal,
A J Black, and
P I Condon, and
B M Gompels, and
R L Green, and
R G Huntsman, and
G C Jenkins
September 1979,
British journal of haematology,
A J Black, and
P I Condon, and
B M Gompels, and
R L Green, and
R G Huntsman, and
G C Jenkins
July 2005,
East African medical journal,
A J Black, and
P I Condon, and
B M Gompels, and
R L Green, and
R G Huntsman, and
G C Jenkins
January 1960,
The British journal of ophthalmology,
A J Black, and
P I Condon, and
B M Gompels, and
R L Green, and
R G Huntsman, and
G C Jenkins
September 2011,
The European respiratory journal,
A J Black, and
P I Condon, and
B M Gompels, and
R L Green, and
R G Huntsman, and
G C Jenkins
September 1959,
Lancet (London, England),
A J Black, and
P I Condon, and
B M Gompels, and
R L Green, and
R G Huntsman, and
G C Jenkins
May 1957,
Journal of clinical pathology,
A J Black, and
P I Condon, and
B M Gompels, and
R L Green, and
R G Huntsman, and
G C Jenkins
December 1964,
The British journal of ophthalmology,
A J Black, and
P I Condon, and
B M Gompels, and
R L Green, and
R G Huntsman, and
G C Jenkins
March 1993,
British journal of haematology,
