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East Afr Med J ; 77(1): 57-9, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10944842

ABSTRACT

Patients with the trichorhinophalangeal syndrome type II, also known as the Langer-Giedion syndrome, may present to the health care-givers or physicians in various specialties and need to be recognised in order that accurate diagnosis, management and counselling about prognosis and recurrence risks may be carried out. A case of young male with this condition is presented.


Subject(s)
Langer-Giedion Syndrome/diagnosis , Langer-Giedion Syndrome/therapy , Child, Preschool , Cytogenetics , Gene Deletion , Genetic Counseling , Humans , Langer-Giedion Syndrome/genetics , Male , Mutation/genetics , Prognosis , South Africa
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