A Child with Cushing's Syndrome – Etiological Clue from Adrenal Imaging (Pediatric Cushing's Syndrome)

Articles in the same Issue

1. Congenital Adrenal Hyperplasia (CAH) a Wolf in a Rabbits' Fur
2. Endogenous Hyperandrogenism and Exercise Capacity Lessons from the Exercise-Congenital Adrenal Hyperplasia Model
3. A Child with Cushing's Syndrome – Etiological Clue from Adrenal Imaging (Pediatric Cushing's Syndrome)
4. Polycystic Ovaries and Adrenal Insufficiency in a Young Pubescent Female with Lipoid Congenital Adrenal Hyperplasia Due to Splice Mutation of the StAR Gene: A Case Report and Review of the Literature
5. Does Fat Fuel the Fire: Independent and Interactive Effects of Genetic, Physiological, and Environmental Factors on Variations in Fat Deposition and Distribution across Populations
6. Application of Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) in Screening of High Risk Children with Inherited Metabolic Diseases in Northern China
7. Relationship Between Aminotransferases Levels and Components of the Metabolic Syndrome Among Multiethnic Adolescents
8. Etiologies of Precocious Puberty: 15-Year Experience in a Tertiary Hospital in Southern Thailand
9. Are IGF-I and IGF-BP3 Useful for Diagnosing Growth Hormone Deficiency in Children of Short Stature?
10. Testosterone, Obesity and Insulin Resistance in Young Males: Evidence for an Association between Gonadal Dysfunction and Insulin Resistance During Puberty
11. Effects of Vitamin D Receptor Gene Polymorphisms on Susceptibility to Disease and Bone Mineral Density in Turkish Patients with Type 1 Diabetes Mellitus
12. Changes in Dynamic Insulin and Gastrointestinal Hormone Secretion in Obese Children
13. Risk Factors for Early Onset of Diabetic Nephropathy in Pediatric Type 1 Diabetes
14. High Frequency of D727E Polymorphisms in Exon 10 of the TSHR Gene in Brazilian Patients with Congenital Hypothyroidism
15. Two Novel Mutations of SRD5A2 Gene in Indonesian Siblings with Clinical 5-Alpha-Reductase Deficiency
16. Serendipitous Identification of Graves' Disease in Identical Twins with Polydipsia
17. The R450H Mutation and D727E Polymorphism of the Thyrotropin Receptor Gene in a Chinese Child with Congenital Hypothyroidism
18. Incidental Finding of Idiopathic Unilateral Adrenal Calcification in an 18-Month-Old Child: Case Report and Review of the Literature