Case Reports

Insulin Oedema in Newly Diagnosed Type 1 Diabetes Mellitus

• Veysel Nijat Baş
• Semra Çetinkaya
• Sebahat Yılmaz Ağladıoğlu
• Havva Nur Peltek Kendirici
• Hatice Bilgili
• Nurdan Yıldırım
• Zehra Aycan

A Patient with 22q11.2 Deletion Syndrome: Case Report

• Sema Kabataş Eryılmaz
• Firdevs Baş
• Ali Satan
• Feyza Darendeliler
• Rüveyde Bundak
• Hülya Günöz
• Nurçin Saka

Case Report

A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make

• Semra Çetinkaya
• Tülay Güran
• Erdal Kurnaz
• Melikşah Keskin
• Elif Sağsak
• Senay Savaş Erdeve
• Jenifer P. Suntharalingham
• Federica Buonocore
• John C. Achermann
• Zehra Aycan

46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin

• Assimina Galli Tsinopoulou
• Anastasios Serbis
• Eleni P. Kotanidou
• Eleni Litou
• Vaia Dokousli
• Konstantina Mouzaki
• Pavlos Fanis
• Vassos Neocleous
• Nicos Skordis

An Unusual Presentation of 46,XY Pure Gonadal Dysgenesis: Spontaneous Breast Development and Menstruation

• Gönül Çatlı
• Caner Alparslan
• P. Şule Can
• Sinem Akbay
• Sefa Kelekçi
• Tahir Atik
• Berk Özyılmaz
• Bumin N. Dündar

Severe Undervirilisation in a 46,XY Case Due to a Novel Mutation in HSD17B3 Gene

• Ayfer Alikaşifoğlu
• Doğuş Vurallı
• Olaf Hiort
• Nazlı Gönç
• Alev Özön
• Nurgün Kandemir

46,XX Male Disorder of Sexual Development: A Case Report

• Ahmet Anık
• Gönül Çatlı
• Ayhan Abacı
• Ece Böber

Gonadoblastoma with Dysgerminoma in a Phenotypically Turner-Like Girl with 45,X/46,XY Karyotype

• Özge Yüce
• Esra Döğer
• Nurullah Çelik
• Hamdi Cihan Emeksiz
• Mahmut Orhun Çamurdan
• Aysun Bideci
• Peyami Cinaz

Review

A Review of the Principles of Radiological Assessment of Skeletal Dysplasias

• Yasemin Alanay
• Ralph S. Lachman

Original Research

Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency

• Erdal Eren
• Tuba Edgünlü
• Emre Asut
• Sevim Karakaş Çelik

Phenotype Heterogeneity in Glucokinase–Maturity-Onset Diabetes of the Young (GCK-MODY) Patients

• Anna Wedrychowicz
• Ewa Tobór
• Magdalena Wilk
• Ewa Ziólkowska-Ledwith
• Anna Rams
• Katarzyna Wzorek
• Barbara Sabal
• Malgorzata Stelmach
• Jerzy B. Starzyk

Letter to Editor

Letter to the Editor regarding “Testotoxicosis: Report of Two Cases, One with a Novel Mutation in Luteinizing Hormone/Choriogonadotropin Receptor Gene”

• Doğa Türkkahraman