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Previous Volume 328:496-502 February 18, 1993 Number 7 Next

	Since this article has no abstract, we have provided an extract of the first 100 words of the full text and any section headings.

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Presentation of Case

A boy six years and two months old was admitted to the hospital because of sexual precocity, polyostotic fibrous dysplasia, and cafe-au-lait spots.

The boy was born after a 37-week, uncomplicated pregnancy to a 23-year-old primigravida; he was delivered by cesarean section because of failure to progress and a decrease in the heart rate noted on the fetal monitor; the birth weight was 2.66 kg. The infant was discharged home at four days with his mother. He reached his milestones at appropriate ages; he walked at 11 months and was toilet-trained at 2 1/2 years. At the ages of three, . . . [Full Text of this Article]

Differential Diagnosis

Clinical Diagnosis

Dr. Joseph A. Majzoub's Diagnosis

Pathological Discussion

Anatomical Diagnoses

Addendum

References

This article has been cited by other articles:

• Coutant, R., Lumbroso, S., Rey, R., Lahlou, N., Venara, M., Rouleau, S., Sultan, C., Limal, J.-M. (2001). Macroorchidism due to Autonomous Hyperfunction of Sertoli Cells and Gs{{alpha}} Gene Mutation: An Unusual Expression of McCune-Albright Syndrome in a Prepubertal Boy. J. Clin. Endocrinol. Metab. 86: 1778-1781 [Abstract] [Full Text]