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SCI-Expanded Vaka Takdimi Scopus
A CASE OF DIABETES MELLITUS TYPE MODY5 AS A FEATURE OF 17Q12 DELETION SYNDROME
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY 2022 Cilt 3 Sayı 2
Scopus Eşleşmesi Bulundu
2
Atıf
16
Cilt
205-210
Sayfa
🔓
Açık Erişim
Scopus Yazarları: Hümeyra Yaşar Köstek, Fatma Özgüç Çömlek, Hakan Gürkan, Emine Neşe Özkayın, Filiz Tütüncüler Kökenli
Özet
Maturity onset diabetes of the young (MODY) is characterized by noninsulin-dependent diabetes diagnosed before the age of 25 years with an autosomal dominant inheritance. Rare mutations in the hepatocyte nuclear factor-1-beta (HNF1B) gene produce a syndrome that resembles MODY. About half of patients diagnosed with MODY type 5 due to HNF1B variants, carry a whole gene deletion, known as 17q12 deletion syndrome. 17q12 deletion syndrome is a rare chromosomal anomaly and is typified by deletion of more than 15 genes, including HNF1B resulting in kidney abnormalities and renal cysts, a diabetes syndrome and neurodevelopmental or neuropsychiatric disorders. A 12-year-old girl was referred after high blood sugar was detected in the hospital where she presented with polyuria and polydipsia, which had persisted for one month. Her serum magnesium (Mg) level was low at 1.5 mg/dL (normal value 1.6-2.6) and glycated hemoglobin was 14% (normal value 3.6-5.8) concurrent with a c-peptide of 1.54 ng/mL (normal value 0.8-4). MODY5 was suspected but the NGS gene panel (ABCC8, BLK, CEL, GCK, HNF1A, HNF1B, HNF4A, INS, KCNJ11, KLF11, NEURODD1, PAX4, PDX1, RFX6, ZFP57, GLIS3, FOXP3, NEUROG3, G6PC2) did not identify any abnormality. During follow-up, her serum Mg remained low (1.2 mg/ dL) together with elevated urinary Mg excretion at 172.5 mg/day. An HNF1B variant was again suspected in a patient with chronic hypomagnesemia with normal basal C peptide level. Abdominal computed tomography and magnetic resonance imaging revealed a 43 mm diameter, cystic lesion in the head of the pancreas, with agenesis of the pancreatic neck, trunk and tail. Genetic testing using a microarray analysis was subsequently performed and a heterozygous deletion at 17q12, including HNF1B, was detected. In case of clinical suspicion of HNF1B variants, further genetic examination using other techniques such as MLPA and CGH array may be required to detect the variant. This is because deletions and duplications may not be detected using next generation screening panel techniques.
Anahtar Kelimeler (Scopus)
17q12 deletion diabetes mellitus hypomagnesemia MODY5
Scimago Dergi Bilgisi Otomatik ISSN Eşleştirmesi 2022 yılı verileri
JCRPE Journal of Clinical Research in Pediatric Endocrinology
Q2
SJR Quartile
0,502
SJR Skoru
50
H-Index
🔓
Açık Erişim
Kategoriler: Pediatrics, Perinatology and Child Health (Q2) · Endocrinology (Q3) · Endocrinology, Diabetes and Metabolism (Q3)
Alanlar: Biochemistry, Genetics and Molecular Biology · Medicine
Ülke: Turkey · Galenos Publishing House
Bu bilgiler makale yılına göre Scimago veritabanından ISSN eşleştirmesiyle otomatik getirilmektedir. Dergi sıralama verileri Scimago'nun ilgili yılı baz alınmaktadır.

Anahtar Kelimeler

17q12 deletion diabetes mellitus hypomagnesemia MODY5

Makale Bilgileri

Dergi JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
ISSN 1308-5727
Yıl 2022 / 12. ay
Cilt / Sayı 3 / 2
Sayfalar 1 – 5
Makale Türü Vaka Takdimi
Hakemlik Hakemli
Endeks SCI-Expanded
Yayın Dili Türkçe
Kapsam Uluslararası
Toplam Yazar 5 kişi
Erişim Türü Elektronik
Erişim Linki Makaleye Git
Alan Sağlık Bilimleri Temel Alanı Çocuk Endokrinolojisi (Çocuk Sağlığı ve Hastalıkları)

YÖKSİS Yazar Kaydı

Yazar Adı YAŞAR KÖSTEK HÜMEYRA, ÖZGÜÇ ÇÖMLEK FATMA, GÜRKAN HAKAN, ÖZKAYIN EMİNE NEŞE, TÜTÜNCÜLER KÖKENLİ FİLİZ
YÖKSİS ID 7784579