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A Case of Klippel-Feil Syndrome with Recurrent Hypoglycemia / 대한소아내분비학회지
Journal of Korean Society of Pediatric Endocrinology ; : 110-115, 2006.
Article in Korean | WPRIM | ID: wpr-224222
ABSTRACT
Klippel-Feil syndrome is characterized by congenital fusion of cervical vertebra which shows classic triad of short neck, low posterior hairline and limited range of motion of the neck. We report a case of Klippel-Feil syndrome not only associated with renal hypoplasia and sensorineural hearing defect but also with repetitive severe hypoglycemia with lactic acidosis.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Spine / Acidosis, Lactic / Range of Motion, Articular / Hearing / Hypoglycemia / Klippel-Feil Syndrome / Neck Language: Korean Journal: Journal of Korean Society of Pediatric Endocrinology Year: 2006 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Spine / Acidosis, Lactic / Range of Motion, Articular / Hearing / Hypoglycemia / Klippel-Feil Syndrome / Neck Language: Korean Journal: Journal of Korean Society of Pediatric Endocrinology Year: 2006 Type: Article