Slipped capital femoral epiphysis: a physeal lesion diagnosed by MRI, with radiographic and CT correlation

1998 ◽  
Vol 27 (3) ◽  
pp. 139-144 ◽  
Author(s):  
H. Umans ◽  
Melissa S. Liebling ◽  
Linda Moy ◽  
Nogah Haramati ◽  
Neil J. Macy ◽  
...  
Keyword(s):  
Slipped Capital Femoral Epiphysis

Slip Progression after in Situ Screw Fixation of Slipped Capital Femoral Epiphysis

PEDIATRICS ◽  
2016 ◽  
Vol 137 (Supplement 3) ◽  
pp. 557A-557A
Author(s):  
Stephanie Chu ◽  
Rachel Y Goldstein ◽  
Erin Dawicki ◽  
Herman Luther ◽  
Lindsay Andras ◽  
...  
Keyword(s):  
Screw Fixation ◽  
Slipped Capital Femoral Epiphysis

The outcome of in situ pinning in treatment of slipped capital femoral epiphysis in adolescents

2019 ◽  
Vol 0 (0) ◽  
pp. 0-0
Author(s):  
Ahmed Akila ◽  
Hossam Khairy ◽  
Mohamed Attia ◽  
ahmed elmalt
Keyword(s):  
Slipped Capital Femoral Epiphysis ◽  
In Situ Pinning

scholarly journals X-linked congenital adrenal hypoplasia: a case presentation

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Hong Ouyang ◽  
Bo Chen ◽  
Na Wu ◽  
Ling Li ◽  
Runyu Du ◽  
...  
Keyword(s):  
Genetic Testing ◽  
Hormone Replacement ◽  
Slipped Capital Femoral Epiphysis ◽  
Clinical Manifestations ◽  
Addison’S Disease ◽  
Addison's Disease ◽  
Case Presentation ◽  
Early Symptoms ◽  
Congenital Adrenal Hypoplasia ◽  
Adrenal Hypoplasia

Abstract Background Most patients with congenital adrenal hypoplasia (AHC) develop symptoms during infantile and juvenile periods, with varying clinical manifestations. AHC is a disease that is easily misdiagnosed as Addison’s disease or congenital adrenal hyperplasia (CAH). There was also a significant time difference between the age at which patients developed symptoms and the age at which they were diagnosed with AHC. Most patients showed early symptoms during infantile and juvenile periods, but were diagnosed with AHC many years later. Case presentation We are currently reporting a male patient who developed systemic pigmentation at age 2 and was initially diagnosed with Addison’s disease. At 22 years of age, he experienced a slipped capital femoral epiphysis (SCFE), a disease mostly seen in adolescents aged 8–15 years, an important cause of which is endocrine disorder. Testes evaluated using color Doppler Ultrasonography suggested microcalcifications. Further genetic testing and auxiliary examinations revealed that the patient had hypogonadotropic hypogonadism (HH) and DAX-1 gene disorders, at which time he was diagnosed with AHC complicated by HH. He was given hormone replacement therapy, followed by regular outpatient review to adjust the medication. Conclusions The typical early symptoms of AHC are hyperpigmentation and ion disturbance during infantile and juvenile periods, while few patients with AHC develop puberty disorders as early symptoms. AHC is prone to being misdiagnosed as Addison’s disease, and then gradually develops the symptoms of HH in adolescence. The definitive diagnosis of AHC ultimately is based on the patient’s clinical presentation, laboratory results and genetic testing results.

Slipped Capital Femoral Epiphysis

1998 ◽  
Vol 7 (1) ◽  
pp. 43-52 ◽  
Author(s):  
R. Velasco ◽  
P. A. Schai ◽  
G. U. Exner
Keyword(s):  
Slipped Capital Femoral Epiphysis

Biomechanical Comparison of Fully and Partially Threaded Screws for Fixation of Slipped Capital Femoral Epiphysis

2008 ◽  
Vol 28 (1) ◽  
pp. 49-52 ◽  
Author(s):  
Firoz Miyanji ◽  
Andrew Mahar ◽  
Richard Oka ◽  
Maya Pring ◽  
Dennis Wenger
Keyword(s):  
Slipped Capital Femoral Epiphysis ◽  
Biomechanical Comparison
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