Spontaneous pneumothorax in association with pyridoxine-responsive homocystinuria

Journal of Inherited Metabolic Disease

Volumn 20, Issue 6, 1997, Pages 831-832

  Bass, H N ^a,b,c   LaGrave, D ^c   Mardach, R ^a,b   Cederbaum, S D ^a,b   Fuster, C D ^a   Chetty, M ^a  

^a KAISER PERMANENTE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c CALIFORNIA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLSALICYLIC ACID; FOLIC ACID; PYRIDOXINE;

ADOLESCENT; ARTICLE; CASE REPORT; EYE DISEASE; HOMOCYSTINURIA; HUMAN; MALE; PATIENT EDUCATION; RECURRENT DISEASE; SPONTANEOUS PNEUMOTHORAX; VASCULAR DISEASE;

ADOLESCENT; HOMOCYSTINE; HOMOCYSTINURIA; HUMANS; MALE; MARFAN SYNDROME; METHIONINE; PNEUMOTHORAX; PYRIDOXINE;

EID: 0030810099     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005384121649     Document Type: Article

References (3)

1. Cochran FB, Sweetman L, Schmidt K, Barsh G, Kraus J, Packman S (1990) Pyridoxine-unresponsive homocystinuria with an unusual clinical course. Am J Med Genet 35: 519-522.
2. McKusick VA (1972) Heritable Disorders of Connective Tissue, 4th edn. St Louis: CV Mosby, 224-281.
3. Mudd SH, Levy HL, Skovby F (1995) Disorders of transsulfuration. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 7th edn. New York: McGraw-Hill, 1279-1327.