Familial Male-limited Precocious Puberty. Case report from Mexico City

被引:0
|
作者
Acosta, Fernanda [1 ]
Zaragoza, Diana [1 ]
Abreu, Melania [2 ]
机构
[1] Issste, Mexico City, Mexico
[2] ABC Med Ctr, Genos Med, Mexico City, Mexico
来源
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
P2-200
引用
收藏
页码:568 / 568
页数:1
相关论文
共 50 条
  • [21] FAMILIAL MALE PRECOCIOUS PUBERTY - A CASE-REPORT TREATED WITH KETOCONAZOLE
    BERTELLONI, S
    BARONCELLI, GI
    FRANCHI, G
    VIACAVA, P
    SAGGESE, G
    RIVISTA ITALIANA DI PEDIATRIA-ITALIAN JOURNAL OF PEDIATRICS, 1994, 20 (03): : 272 - 275
  • [22] Management with five antihypertensives in patient with precocious puberty. Case report
    Camila Ruiz-Rivera, Maria
    Clemente Mendoza-Rojas, Victor
    IATREIA, 2018, 31 (03) : 305 - 311
  • [23] Heterogeneity of activating mutations of the human luteinizing hormone receptor in male-limited precocious puberty
    Laue, L
    Wu, SM
    Kudo, M
    Hsueh, AJW
    Cutler, GB
    Jelly, DH
    Diamond, FB
    Chan, WY
    BIOCHEMICAL AND MOLECULAR MEDICINE, 1996, 58 (02) : 192 - 198
  • [24] Hypothalamic hamartoma causing precocious puberty.: Report of one case
    Alvarado, J
    López, JM
    REVISTA MEDICA DE CHILE, 2001, 129 (10) : 1179 - 1182
  • [25] Six-year results of spironolactone and testolactone treatment of familial male-limited precocious puberty with addition of deslorelin after central puberty onset
    Leschek, EW
    Jones, J
    Barnes, KM
    Hill, SC
    Cutler, GB
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (01): : 175 - 178
  • [26] Long-term outcome of male-limited gonadotropin-independent precocious puberty
    Bertelloni, S
    Baroncelli, GI
    Lala, R
    Cappa, M
    Matarazzo, P
    DeSanctis, C
    Saggese, G
    HORMONE RESEARCH, 1997, 48 (05) : 235 - 239
  • [27] A missense (T577I) mutation in the luteinizing hormone receptor gene associated with familial male-limited precocious puberty
    Cocco, S
    Meloni, A
    Marini, MG
    Cao, A
    Moi, P
    HUMAN MUTATION, 1996, 7 (02) : 164 - 166
  • [28] GENETIC-HETEROGENEITY OF CONSTITUTIVELY ACTIVATING MUTATIONS OF THE HUMAN LUTEINIZING-HORMONE RECEPTOR IN FAMILIAL MALE-LIMITED PRECOCIOUS PUBERTY
    LAUE, L
    CHAN, WY
    HSUEH, AJW
    KUDO, M
    HSU, SY
    WU, SM
    BLOMBERG, LA
    CUTLER, GB
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (06) : 1906 - 1910
  • [29] Substitution of M398T in the second transmembrane helix of the LH receptor in a patient with familial male-limited precocious puberty
    Ignacak, M
    Hilczer, M
    Zarzycki, J
    Trzeciak, WH
    ENDOCRINE JOURNAL, 2000, 47 (05) : 595 - 599
  • [30] A case series of 2 pediatric patients with precocious puberty due to familial male limited testotoxicosis
    Ubico, E. E. Morales
    Lim, W.
    AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2025, 369