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SCI-Expanded JCR Q4 Vaka Takdimi Scopus
A RARE ASSOCIATION OF MONOSOMY 18p SYNDROME AND POLYGLANDULAR AUTOIMMUNE SYNDROME TYPE IIIA
BALKAN JOURNAL OF MEDICAL GENETICS 2013 Cilt 16 Sayı 1
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

Metrikler

Scopus Atıf 1
JCR Quartile Q4
Yazar Sayısı 5