Lost to follow-up in classic congenital adrenal hyperplasia: a case report

2019 ◽  
Author(s):  
Costa Cristiana Gomes da ◽  
Tania Matos ◽  
Vale Sonia do
Keyword(s):  
Case Report ◽  
Congenital Adrenal Hyperplasia ◽  
Adrenal Hyperplasia ◽  
Classic Congenital Adrenal Hyperplasia ◽  
Lost To Follow Up

Non-classic congenital adrenal hyperplasia: Case report

2019 ◽  
Vol 493 ◽  
pp. S252
Author(s):  
R. LÓpez Travieso ◽  
M.D. MartÍn MartÍnez ◽  
E. Mateos RodrÍguez ◽  
J.M. Barrasa FernÁndez ◽  
A. FernÁndez Ferreiro
Keyword(s):  
Case Report ◽  
Congenital Adrenal Hyperplasia ◽  
Adrenal Hyperplasia ◽  
Classic Congenital Adrenal Hyperplasia

scholarly journals Management of Non-Classic Congenital Adrenal Hyperplasia in Pregnant Woman - Non-Referral Center Experience- Case Report

2019 ◽  
Vol 6 (2) ◽  
Author(s):  
Gluvic Zoran ◽  
Lackovic Milena ◽  
Samardzic Vladimir ◽  
Mitrovic Bojan ◽  
Mladenovic Violeta ◽  
...  
Keyword(s):  
Case Report ◽  
Pregnant Woman ◽  
Congenital Adrenal Hyperplasia ◽  
Adrenal Hyperplasia ◽  
Referral Center ◽  
Classic Congenital Adrenal Hyperplasia

scholarly journals Severe Hirsutism in Non Classic Congenital Adrenal Hyperplasia: A Case Report and Literature Review

2020 ◽  
Vol 8 (C) ◽  
pp. 8-11
Author(s):  
Merita Emini ◽  
Blertina Olldashi ◽  
Blerina Qovanaj
Keyword(s):  
Case Report ◽  
Congenital Adrenal Hyperplasia ◽  
Hair Loss ◽  
Adrenal Hyperplasia ◽  
Clinical Appearance ◽  
Classic Congenital Adrenal Hyperplasia ◽  
Female Pattern Hair Loss ◽  
History Of ◽  
Grade Ii ◽  
Classic Form

   BACKGROUND: Non-classic congenital adrenal hyperplasia (NCAH) is a relatively common disorder, but very often, it remains undiagnosed. Clinical appearance of NCAH can be asymptomatic at birth. Symptoms are presented more often in late childhood, adolescence, or later in life caused by excessive androgen secretion. CASE REPORT: We report the case of 27-year-old girl with 2 years history of high-grade of hirsutism, hair loss on the front of scalp with female pattern hair loss, (grade II according to Ludwig scale), breast volume reduction, weight loss (15 kg), depression, but without menstrual disorders, normal blood pressure, and usage of oral contraceptives for more than 1 year without any improvement. We did blood tests for hormonal protocol for hyperandrogenemia and we found these values high 17 (OH) progesterone and all other androgen hormones. After these examinations, the patient was diagnosed with a non-classic form of CAH. CONCLUSION: Treatment with corticosteroids and other necessary treatment improved clinical and hormonal features.  

Combination of turner syndrome and congenital adrenal hyperplasia: a rare case report

2017 ◽  
Author(s):  
Ivana Sagova ◽  
Dušan Pavai ◽  
Matej Stančik ◽  
Helena Urbankova ◽  
Juliana Gregova ◽  
...  
Keyword(s):  
Case Report ◽  
Congenital Adrenal Hyperplasia ◽  
Turner Syndrome ◽  
Rare Case ◽  
Adrenal Hyperplasia ◽  
Rare Case Report

Bioelectrical Impedance Phase Angle and Its Determinants in Patients with Classic Congenital Adrenal Hyperplasia

2021 ◽  
pp. 1-8
Author(s):  
Núbia Maria de Oliveira ◽  
Raquel David Langer ◽  
Sofia Helena Valente de Lemos-Marini ◽  
Gil Guerra-Júnior ◽  
Ezequiel Moreira Gonçalves
Keyword(s):  
Congenital Adrenal Hyperplasia ◽  
Phase Angle ◽  
Bioelectrical Impedance ◽  
Adrenal Hyperplasia ◽  
Classic Congenital Adrenal Hyperplasia
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