Suzan Alexander

Summary

Publications

  1. ncbi request reprint Homozygous mutation of P450 side-chain cleavage enzyme gene (CYP11A1) in 46, XY patient with adrenal insufficiency, complete sex reversal, and agenesis of corpus callosum
    Hessa al Kandari
    King Fahad Hospital, King Abdul Aziz Medical City, P O Box 22490, Pediatric Department 1510, Riyadh 11426, Kingdom of Saudi Arabia
    J Clin Endocrinol Metab 91:2821-6. 2006
  2. doi request reprint Familial glucocorticoid deficiency in five Arab kindreds with homozygous point mutations of the ACTH receptor (MC2R): genotype and phenotype correlations
    Hessa M Al Kandari
    Department of Pediatrics, Farwaniya Hospital, Kuwait
    Horm Res Paediatr 76:165-71. 2011

Collaborators

  • N Katsumata
  • Hessa M Al Kandari
  • Hessa al Kandari
  • Mohammed Al Balwi
  • Majedah S Abdul Rasoul
  • Ibrahim Al Alwan
  • Majedah Abdul Rasoul

Detail Information

Publications2

  1. ncbi request reprint Homozygous mutation of P450 side-chain cleavage enzyme gene (CYP11A1) in 46, XY patient with adrenal insufficiency, complete sex reversal, and agenesis of corpus callosum
    Hessa al Kandari
    King Fahad Hospital, King Abdul Aziz Medical City, P O Box 22490, Pediatric Department 1510, Riyadh 11426, Kingdom of Saudi Arabia
    J Clin Endocrinol Metab 91:2821-6. 2006
    ..Defective enzyme activity leads to the deficiency of all steroid hormones, including progesterone, which is essential to sustain term pregnancy...
  2. doi request reprint Familial glucocorticoid deficiency in five Arab kindreds with homozygous point mutations of the ACTH receptor (MC2R): genotype and phenotype correlations
    Hessa M Al Kandari
    Department of Pediatrics, Farwaniya Hospital, Kuwait
    Horm Res Paediatr 76:165-71. 2011
    ..To date, hypothyroidism has been reported as an associated feature in a few cases. The clinical findings along with MC2R genetic analysis of five Arab kindreds are described...