An interesting case of familial chylomicronemia syndrome in a cleft palate child

H. S. Adenwalla; P. V. Narayanan; C. J. Rajshree; Rati Santhakumar

doi:10.4103/0970-0358.41116

Indian Journal of Plastic Surgery, Inhaltsverzeichnis

CC BY-NC-ND 4.0 · Indian J Plast Surg 2008; 41(01): 70-72
DOI: 10.4103/0970-0358.41116

Case Report

Association of Plastic Surgeons of India

An interesting case of familial chylomicronemia syndrome in a cleft palate child

Autor*innen

H. S. Adenwalla

Departments of Plastic Surgery
P. V. Narayanan

Departments of Plastic Surgery
C. J. Rajshree

Departments of Plastic Surgery
Rati Santhakumar

¹Pediatrics and Burns, Charles Pinto Centre for Cleft Lip, Palate and Craniofacial Anomalies,Jubilee Mission Medical College and Research Institute, Trichur - 680 005, Kerala, India

Abstract

als PDF herunterladen

ABSTRACT

familial chylomicronemia syndrome is a very rare condition with an incidence of one in one million. we report such a condition detected incidentally in a cleft child.

KEYWORDS

Familial hyperlipoprotenemia - lipoprotein lipase

PDF (88 kb)

Referenzen

1 Rifai N, Warnick RG. Lipids, lipoproteins, apolipoproteins and other cardiovascular risk factors. TIETZ Textbook of Clinical Chemistry and Molecular Diagnostics: 2006. p. 929,935,938.
2 Henderson RA, Rinker AD. Gastric, pancreatic and intestinal function. TIETZ Text book of Clinical Chemistry: 1998. p. 1310.
3 Mahley RW, Weisgreber KH, Farese RV Jr. Disorders of lipid metabolism. 10 th ed. Williams Textbook of Endocrinology: 1675.
4 Rader DJ, Hobbs HH. Disorders of lipid metabolism. Harrisons Principles of Internal Medicine. 16 th ed. 2289.
5 Tershakove AM, Rader DJ. Defects in metabolism and lipids; 75.3 - Disorders of Lipoprotein metabolism and Transport. Nelsons Textbook of Pediatrics, 17 th ed. p. 448.