Síndrome de Woodhouse Sakati / Woodhouse-Sakati syndrome: a case report
An. Fac. Med. (Perú)
; 69(4): 260-262, oct.-dic. 2008. ilus
Article
in Spanish
| LILACS, LIPECS
| ID: lil-564589
Responsible library:
PE1.1
RESUMEN
Presentamos un caso de síndrome de Woodhouse Sakati, en una paciente de11 años de edad, quien presentó alopecia congénita, hipoacusia neurosensorial bilateral, diabetes mellitus insulino dependiente, hipogonadismo primario, retardo del desarrollo psicomotor, comunicación interventricular y disminución de somatomedina C (IGF1). La evolución y el tratamiento de soporte fueron satisfactorios.
ABSTRACT
We present a rare case of Woodhouse-Sakati syndrome in an 11 year-old patient, who presented congenital alopecia, bilateral sensorineural hearing loss, insulindependent diabetes mellitus, primary hypogonadism, psychomotor retardation, interventricular communication, decreased IGF1. The evolution and supportive treatment were satisfactory.
Full text:
Available
Collection:
National databases
/
Peru
Database:
LILACS
/
LIPECS
Main subject:
Receptor, IGF Type 1
/
Diabetes Mellitus
/
Alopecia
/
Hypogonadism
/
Multiple Organ Failure
Limits:
Child
/
Female
/
Humans
Language:
Spanish
Journal:
An. Fac. Med. (Perú)
Year:
2008
Document type:
Article
Institution/Affiliation country:
Instituto Nacional de Salud del Niño/PE
/
Seguro Social de Salud-EsSalud/PE
