Erken Bulgu Veren ancak Geç Tanı Konulan Bir Olgu; Ataksi Telenjiektazi

Yıl 2020, Cilt: 9 Sayı: 1, 63 - 66, 30.04.2020

Hilal Aydin , İbrahim Hakan Bucak , Haydar Bagis

Öz

Ataksi-telenjiektazi hastalığı otozomal resesif genetik geçiş gösteren nörodejeneratif bir hastalıktır. Bu hastalığın ana bulgusu ilk yaşlarda ortaya çıkan trunkal ataksidir. Bakış kısıtlılığı şikayeti ile başvuran on bir yaşında erkek hastada dengesiz yürüme ve peltek konuşma tespit edildi. Hastada mental gerilik, dizartrik konuşma, trunkal ataksi, başta titubasyon, ellerde intansiyel tremor, horizantal/vertikal nistagmus, yüzde ve sklerada telenjiektazik damarlar, yukarı laterale bakış dışında diğer alanlarda bakış kısıtlılığı, dismetri, disdiadokinezi, kaba yüz görünümü olduğu belirlendi. Kranial magnetik rezonans görüntülemesinde her iki serebeller hemisferde atrofi tespit edildi. Alfa fetoprotein değeri 38 ng/ml (0.9-7.6) ile yüksekti. Ataksi Telenjiektazi ATM geni mutasyon analizinde 25. ekzonunda bulunan p.Lys1192Lys (c.3576 G>A) değişimini homozigot olarak saptandı. Ataksi, nöromotor retardasyon, telenjektazi ve göz bulgularının olduğu hastalarda Ataksi-telenjiektazi hastalığı ilk akla gelen tanılardan biri olmalıdır. 

Anahtar Kelimeler

Ataksi Telenjiektazi, nistagmus, ayırıcı tanı

A Case Giving Early Findings, But Diagnosed Late: Ataxia Telangiectasia

Öz

Ataxia telangiectasia is a neurodegenerative disease exhibiting autosomal recessive genetic transmission. The principal finding of the disease is truncal ataxia emerging in the first years. Gait imbalance and lisp were determined in an 11-year-old boy presenting due to gaze restriction. Mental retardation, dysarthric speech, truncal ataxia, titubation of the head, intention tremor in the hands, horizontal/vertical nystagmus, telangiectasia in the face/sclera, restriction in all gaze fields except for upward lateral, dysmetria, dysdiadochokinesia, and a coarse facial appearance were observed. Cranial magnetic resonance imaging revealed atrophy cerebral hemispheres. Alpha fetoprotein was elevated, at 38 ng/ml (0.9-7.6). Ataxia telangiectasia ATM gene mutation analysis reported a homozygous p.Lys1192Lys (c.3576 G>A) change on the 25^th exon. This case report is intended to emphasize that ataxia telangiectasia should be the first condition considered at differential diagnosis in patients with ataxia, neuromotor retardation, telangiectasia, and ocular findings. 

Anahtar Kelimeler

Ataxia Telangiectasia, nystagmus, differential diagnosis

Kaynakça

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