Aplastic anaemia in association with Kearns-Sayre syndrome

Journal of Inherited Metabolic Disease

Volumn 22, Issue 1, 1999, Pages 86-87

  Leung, T F ^a   Hui, J ^a   Shoubridge, E ^b   Li, C K ^a   Chik, K W ^a   Shing, M M K ^a   Wong, G W K ^a   Yeung, W L ^a   Yuen, P M P ^a  

^a CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CALCITRIOL; CALCIUM ION; HEMOGLOBIN; PARATHYROID HORMONE;

APLASTIC ANEMIA; ARTICLE; BONE MARROW BIOPSY; CALCIUM BLOOD LEVEL; CASE REPORT; DISEASE ASSOCIATION; DISEASE COURSE; ERYTHROPOIESIS; FEMALE; GROWTH HORMONE DEFICIENCY; HORMONE SUBSTITUTION; HUMAN; HYPOCALCEMIA; HYPOPARATHYROIDISM; HYPOPHOSPHATEMIA; KEARNS SAYRE SYNDROME; LEUKOCYTE COUNT; MUSCLE BIOPSY; NEUTROPHIL; NUCLEAR MAGNETIC RESONANCE IMAGING; PANCYTOPENIA; PARATHYROID HORMONE BLOOD LEVEL; RETICULOCYTE COUNT; SCHOOL CHILD; SOUTHERN BLOTTING; THROMBOCYTE COUNT;

ANEMIA, APLASTIC; CHILD; FEMALE; HUMANS; KEARNS-SAYER SYNDROME;

EID: 0033055543     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005415802893     Document Type: Article

References (3)

1. Harding AE, Hammans SR (1992) Deletions of the mitochondrial genome. J Inher Metab Dis 15: 480-486.
2. Kerr DS (1997) Protean manifestations of mitochondrial diseases: a minireview. J. Pediatr Hematol Oncol 19: 279-286.
3. Shoffner JM, Wallace DC (1995) Oxidative phosphorylation diseases. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 7th edn. New York: McGraw-Hill, 1535-1609.