MATERIALSAND METhODS Twenty-two females, age 2 to 14 yr (mean ±sd= 5.9 ±3 yr),
were diagnosed as having the McCune-Albright syndrome based on the presence of …

Bone scintigraphy proved valuable in diagnosing McCune-Albright's syndrome in a 6-year-
old girl by detecting multiple, non-symptomatic foci in the skull, axial skeleton and in the …

McCune-Albright syndrome consists of polyostotic fibrous dysplasia, precocious puberty and
caje-au-lait skin lesions. Bone lesions are characterized by the presence of fibrous …

We report the diagnostic clinical features and their long term evolution in 32 patients with
McCune-Albright syndrome. Patient data are made up of two periods: the first, classified as …

Abstract The McCune Albright syndrome is characterized in complete form by (a) patchy
areas of a particular type of progressive bone disease termed polyostotic fibrous …

In 1937, McCune and Bruch1 and Albright and associates2 separately described an
unusual syndrome characterized by polyostotic fibrous dysplasia, café au lait pigmentation …

This article describes clinical follow-up of 15 patients—13 females and two males—with
McCune-Albright syndrome. Osseous fractures occurred only during childhood, while …

McCune-Albright syndrome was diagnosed at 2.5 years in a male, with a lower limb fracture
and cafe-au-lait markings. Polyostotic fibrous dysplasia was treated with Pamidronate for 4 …

This paper is a detailed case study of a seven‐year‐old girl who developed precocious
puberty. The young girl experienced bilateral breast enlargement, vaginal discharge, and …

ABSTRACT The diagnosis of McCune-Albright syndrome has classically consisted of the
triad of gonadotropin-independent precocious puberty (GIPP), cafe-au-lait (CAL) spots and …