Hypokolemic paralysis and megaloblastic anaemia in laurence-moon-bardet-biedl syndrome
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2009; 19 (3): 186-188
en Inglés
| IMEMR
| ID: emr-91629
ABSTRACT
Laurence-Moon-Bardet-Biedl syndrome is a rare, genetically heterogeneous autosomal recessive disorder, characterized by progressive retinal dystrophy, polydactyly, obesity, hypogonadism, mental retardation, and renal dysfunction. Other manifestations include diabetes mellitus, heart disease, hepatic fibrosis and neurological features. Herein, 2 patients with Laurence-Moon-Bardet-Biedl syndrome are described, who had features of persistent hypokalemia and megaloblastic anemia
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Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Parálisis Periódica Hipopotasémica
/
Síndrome de Bardet-Biedl
/
Hipopotasemia
/
Anemia Megaloblástica
Tipo de estudio:
Informe de Casos
Límite:
Humanos
/
Masculino
Idioma:
Inglés
Revista:
J. Coll. Physicians Surg. Pak.
Año:
2009
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