Scopus Eşleşmesi Bulundu
1
Atıf
16
Cilt
81-84
Sayfa
🔓
Açık Erişim
Scopus Yazarları: D. Dolek-Cetinkaya, Mustafa Demirpençe, Ahmet Gorgel, Fusun Salgur, Mitat Bahçeci
Özet
We report a monosomy 18p syndrome in a male patient with polyglandular autoimmune syndrome (PAS) type IIIA. A 34-year-old mentally retarded diabetic male patient with short stature, wide earlaps, old-looking face, straight nasal bone, atrophic mouth, drooping cheeks, full teeth loss, and soft, weak and sparse white hair was admitted to the outpatient endocrinology clinic. Chromosome analysis of the patient revealed 46,XY,del(18)(p11.2). He was also diagnosed with autoimmune thyroiditis, primary hypothyroidism and diabetes mellitus type 1. We concluded that monosomy 18p syndrome may be associated with autoimmune diseases and if this is suspected, patients should be examined for an endocrine deficiency.
Anahtar Kelimeler (Scopus)
Growth hormone deficiency
Type 1 diabetes and hypothyroidism
Hypogo-nadotropic hypogonadism
Monosomy 18p
Anahtar Kelimeler
Monosomy 18p
Type 1 diabetes and hypothyroidism
Growth hormone deficiency
Hypogo-nadotropic hypogonadism
Makale Bilgileri
Dergi
BALKAN JOURNAL OF MEDICAL GENETICS
ISSN
1311-0160
Yıl
2013
/ 1. ay
Cilt / Sayı
16
/ 1
Makale Türü
Vaka Takdimi
Hakemlik
Hakemli
Endeks
SCI-Expanded
JCR Quartile
Q4
Yayın Dili
İngilizce
Kapsam
Uluslararası
Toplam Yazar
5 kişi
Erişim Türü
Elektronik
Erişim Linki
Makaleye Git
Alan
Sağlık Bilimleri Temel Alanı
Endokrinoloji ve Metabolizma Hastalıkları (İç Hastalıkları)
Monosomy 18p, Type 1 diabetes and hypothyroidism, Growth hormone deficiency, Hypogo-nadotropic hypogonadism
YÖKSİS Yazar Kaydı
Yazar Adı
DÖLEK ÇETİNKAYA DEVRİM, DEMİRPENÇE MUHAMMED MUSTAFA, GÖRGEL AHMET, SALGÜR FÜSUN, BAHÇECİ MİTAT
YÖKSİS ID
7788383
Hızlı Erişim
Metrikler
Scopus Atıf
1
JCR Quartile
Q4
Yazar Sayısı
5