Infant cholestasis in McCune-Albright syndrome [2]

Acta Paediatrica, International Journal of Paediatrics

Volumn 93, Issue 1, 2004, Pages 141-

  El Rifai, N ^a   Lumbroso, S ^b   Cartigny, M ^a   Weill, J ^a   Sultan, C ^b   Gottrand, F ^a  

^a LILLE UNIVERSITY HOSPITAL   (France)

^b LAPEYRONIE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

URSODEOXYCHOLIC ACID;

ALBRIGHT SYNDROME; ANAMNESIS; CASE REPORT; CHILD; CHOLESTASIS; CLINICAL FEATURE; DIAGNOSTIC APPROACH ROUTE; DIAGNOSTIC TEST; DISEASE COURSE; FEMALE; HISTOPATHOLOGY; HUMAN; LABORATORY TEST; LETTER; LIVER BIOPSY; MEDICAL EXAMINATION; PRIORITY JOURNAL; TREATMENT OUTCOME;

EID: 9144248945     PISSN: 08035253     EISSN: None     Source Type: Journal    
DOI: 10.1080/08035250310007880     Document Type: Letter

References (6)

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2. Weinstein LS, Shenker A, Gejman PV, Merino MJ, Friedman E, Spiegel AM. Activating mutations of the stimulatory G protein in the McCune-Albright syndrome. N Engl J Med 1991; 325: 1688-95
3. Shenker A, Weinstein LS, Moran A, Pescovitz OH, Charest NJ, Boney CM, et al. Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein Gs. J Pediatr 1993; 123: 509-18
4. Lumbroso S, Paris F, Sultan C. McCune-Albright syndrome: molecular genetics. J Pediatr Endocrinol Metabol 2002; 15: 875-82
5. Grumbach MM, Styne DM. Puberty: ontogeny, neuroendocrinology, physiology, and disorders. In: Wilson JD, Foster DW, Kronenberg HM, Larsen PR, editors. Williams textbook of endocrinology. 9th ed. Philadelphia: WB Saunders 1998: 1590-2
6. Rieger E, Kofler R, Borkenstein M, Schwingshandl J, Soyer HP, Kerl H. Melanotic macules following Blashko's lines in McCune-Albright syndrome. Br J Dermatol 1994; 130: 215-20