Diagnosis of late puberty

Hormone Research

Volumn 51, Issue SUPPL. 3, 1999, Pages 95-100

  Argente, Jesús ^a  

^a HOSPITAL INFANTIL UNIVERSITARIO NIÑO JESÚS   (Spain)

Author keywords

Chronic illness; Constitutional delay of puberty; Delayed puberty; Late puberty; Puberty

Indexed keywords

GONADOTROPIN; GROWTH FACTOR; GROWTH HORMONE; PROLACTIN; SEX HORMONE; THYROID HORMONE;

BODY HEIGHT; BONE MATURATION; BREAST DEVELOPMENT; CHILD GROWTH; CHRONIC DISEASE; CONFERENCE PAPER; DELAYED PUBERTY; EATING DISORDER; ENDOCRINE DISEASE; FEMALE; GENETIC DISORDER; HORMONE BLOOD LEVEL; HUMAN; HYPOGONADOTROPIC HYPOGONADISM; KARYOTYPE; MALE; MALNUTRITION; NUCLEAR MAGNETIC RESONANCE IMAGING; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SHORT STATURE; TUMOR;

EID: 0032718821     PISSN: 03010163     EISSN: None     Source Type: Journal    
DOI: 10.1159/000053168     Document Type: Conference Paper

References (31)

1. Styne DM: New aspects in the diagnosis and treatment of pubertal disorders. Pediatr Clin North Am 1997;44:505-529.
2. Pozo J, Argente J: Retraso constitucional del crecimiento y de la adolescencia. Endocrinología 1994;41:60-68.
3. Cara JF, Rosenfield RL: Insulin-like growth factor I and insulin potentiate luteinizing hormone-induce androgen synthesis by rat ovarian theca-interstitial cells. Endocrinology 1988; 123:733-739.
4. Bertelloni S. Baroncelli GI, Ferdeghini M, Perri G, Saggese G: Normal volumetric bone mineral density and bone turnover in young men with histories of constitutional delay of puberty. J Clin Endocrinol Metab 1998;83:4280-4283.
5. Moreira-Andrés MN, Cañizo FJ, de la Cruz FJ, Gómez de la Cámara A, Hawkins FG: Bone mineral status in prepubertal children with constitutional delay of growth and puberty. J Clin Endocrinol Metab 1998;139:271-275.
6. Saenger P, Sandberg DE: Delayed puberty: when to wake the bugler. J Pediatr 1998;133: 724-726.
7. Rodríguez-Hierro F: Pubertad retrasada; in Argente J, Carrascosa A, Gracia R, Rodriguez-Hierro F (eds): Tratado de Endocrinología Pediátrica y de la Adolescencia. Madrid, Edimsa, 1995, pp 713-730.
8. Oberger E, Engström I, Karlberg J: Long-term treatment with glucocorticoids/ACTH in asthmatic children. III. Effects on growth and adult height. Acta Pædiatr Scand 1990;79:77-83.
9. Preece MA, Low CM, Davies PSW: The growth of children with chronic pediatric diseases. Clin Endocrinol Metab 1986;15:453-477.
10. Booth IW: Nutritional consequences of gastrointestinal disease in adolescence. Acta Pædiatr Scand 1991;373:91-102.
11. Handelsman DJ, Dong Q: Hypothalamic-pituitary-gonadal axis in chronic renal failure. Endocrinol Metab Clin North Am 1993;22:145-161.
12. Hokken AC, van Doorn JW, Hahlen K, Stijnen T, de Muinck SM, Drop SL: Long-term effects of treatment for acute lymphoblastic leukemia with and without cranial irradiation on growth and puberty: a comparative study. Pediatr Res 1993;33:577-582.
13. Borgna-Pignatti C, De Stefano P, Zonta L, Vullo C, De Sanctis V, Melevendi C, Naselli A, Masera G, Terzoli S, Gabutti Y: Growth and sexual maturation in thalassemia major. J Pediatr 1985;106:150-155.
14. Muñoz MT, Morandé G, Argente J: Anomalías en el patrón de secreción de gonadotrofinas en las pacientes afectas de anorexia nervosa. Endocrinologia 1997;44:248-252.
15. Warrem MP: The effect of exercise in pubertal progression and reproductive functions in girls. J Clin Endocrinol Metab 1980;51:1150-1157.
16. Hardelin JP, Levilliers J, Young J, Pholsena M, Legouis R, Kirk J, Bouloux P, Petit C, Schaison G: Xp22.3 deletions in isolated familial Kallmann's syndrome. J Clin Endocrinol Metab 1993;76:827-831.
17. Burris TP, Guo W, McCabe ERB: The gene responsible for adrenal hypoplasia congenita, DAX-1, encodes a nuclear hormone receptor that defines a new class within the superfamily. Recent Prog Horm Res 1996;51:241-260.
18. Zachmann M, Fuchs E, Prader A: Progressive high frequency hearing loss - an additional feature in the syndrome of congenital adrenal hypoplasia and gonadotrophin deficiency. Eur J Pediatr 1992;151:167-169.
19. Layman LC, Lee EJ, Peak DB, Nammoum AB, Vu KV, van Lingen NL, Gray MR, McDonough PG, Reindollar RH, Jameson JL: Delayed puberty and hypogonadism caused by mutations in the follicle-stimulating hormone beta-subunit gene. N Engl J Med 1997;337:607-611.
20. Weiss J, Axelrod L, Whitcomb RW, Harris PE, Crowley WF, Jameson JL: Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone. N Engl J Med 1992;326:179-183.
21. Wu W, Cogan JD, Pfäffle RW, Dasen JS, Frisch H, O'Connell SM, Flynn SE, Brown MR, Mullis PE, Parks JS, Phillips JA: Mutations in PROP1 cause familial combined pituitary hormone deficiency. Nat Genet 1998;18: 147-149.
22. Dattani MT, Martínez-Barbera JP, Thomas PQ, Brickman JM, Gupta R, Martensson IL, Toresson H, Fox M, Wales JK, Hindmarsh PC, Krauss S, Beddington RS, Robinson IC: Mutations in the homeobox gene HESX1/Hesxl associated with septo-optic dysplasia in human and mouse. Nat Genet 1998;19:125-133.
23. Kirkilionis A, Gregory CA, Hamerton JL: Long-range restriction mapping and linkage analysis of the Prader-Willi chromosome region (PWCR). Genomics 1991;9:524-535.
24. Banna M, Hoare RD, Stanley P: Craniopharyngioma in children. J Pediatr 1973;83:781-785.
25. Mootha SL, Barkovich AJ, Grumbach MM, Edwards MS, Gitelman SE, Kaplan SL, Conte FA: Idiopathic hypothalamic diabetes insipidus, pituitary stalk thickening, and the occult intracranial germinoma in children and adolescents. J Clin Endocrinol Metab 1997;82:1362-1367.
26. Willman CL, Busque L, Griffith BB, Favara BE, McClain KL, Duncan MH, Gilliland DG: Langerhans cell histiocytosis (histiocytosis X)- a clonal proliferative disease. N Engl J Med 1994;331:154-160.
27. Richards GE, Wara WM, Grumbach MM, Kaplan SL, Sheline GE, Conte FA: Delayed onset of hypopituitarism: sequelae of therapeutic irradiation of central nervous system, eye and middle ear tumors. J Pediatr 1976;89:553-559.
28. Rosenfeld RG, Grumbach MM: Turner Syndrome. New York, Marcel Dekker, 1990.
29. Latronico AC, Anasti J, Arnhold IJP, Rapaport R, Mendonca BB, Bloise W, Castro M, Tsigos C, Chrousos GP: Brief report: testicular and ovarian resistance to luteinizing hormone caused by homozygous inactivating mutations of the luteinizing hormone receptor gene. N Engl J Med 1996;334:507-512.
30. Aitomaki K, Herva R, Stennman U-H, Juntunen K, Ylostato P, Hovatta O, Chapelle A: Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene. J Clin Endocrinol Metab 1996;81:3722-3726.
31. Jasmieson CR, van der Burgt I, Brady AF, van Reen M, Elsawi MM, Hol F, Jeffery S, Patton MA, Mariman E: Mapping a gene for Noonan syndrome to the long arm of chromosome 12. Nat Genet 1994;8:357-360.