TY  - JOUR
T1  - FAbry's disease with hypogammaglobulinemia and without angiokeratomas
AU  - Urbain G, Philippart M, Peremans J
Y1  - 1969/07/01
N1  - 10.1001/archinte.1969.00300170074014
JO  - Archives of Internal Medicine
SP  - 72
EP  - 76
VL  - 124
IS  - 1
N2  - The differential diagnosis of the lipid storage diseases rests on a variety of clinical, histological, and biochemical findings. Only biochemical analyses of the stored lipids can provide comprehensive classification. This is illustrated in the report to follow. Several remarkable features in this patient's illness were (1) the absence of typical skin lesions; (2) an associated hypogammaglobulinemia, and (3) diagnosis which could only be made by biochemical studies.Patient Summary 
    A 23-year-old white man had a fever of unknown origin and was admitted to the Belgian Army Hospital in June 1965. In 1959, at the age of 17, he had an episode of acute colitis with hematochezia. He was treated with chloromycetin and was free of symptoms after two weeks. In 1964, he consulted a physician because of dyspnea and fatigue occurring with exercise. No clinical abnormalities were found other than a low-grade systolic murmur. A few months later, the patient
SN  - 0003-9926
M3  - doi: 10.1001/archinte.1969.00300170074014
UR  - http://dx.doi.org/10.1001/archinte.1969.00300170074014
ER  -