Progressive cerebellar ataxia with extensive peripheral telangiectasias in ataxia-telangiectasia

We present a school-aged girl with ataxia-telangiectasia (AT), a rare autosomal recessive neurodegenerative disorder. She presented with progressive cerebellar ataxia beginning at 12 months, ocular telangiectasias developing at 4 years and unusually extensive cutaneous telangiectasias on the dorsum of hands, feet and limbs emerging at 5 years. Laboratory investigations revealed elevated alpha-fetoprotein levels, decreased immunoglobulin A and G and cerebellar atrophy on MRI. The patient experienced recurrent sinopulmonary infections requiring monthly intravenous immunoglobulin therapy. This patient demonstrates the classical neurological manifestations of AT alongside an atypical distribution of prominent cutaneous telangiectasias, emphasising the importance of early recognition for appropriate management and genetic counselling.

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Publication Details

Journal
BMJ Case Reports
Published
2025-12-01
DOI
https://doi.org/10.1136/bcr-2025-269367
Primary Topic
DNA Repair Mechanisms
Type
article
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article

Progressive cerebellar ataxia with extensive peripheral telangiectasias in ataxia-telangiectasia

Yagiz Alp Aksoy, Gizem Öztürk
BMJ Case Reports
DNA Repair Mechanisms
article

Progressive cerebellar ataxia with extensive peripheral telangiectasias in ataxia-telangiectasia

Yagiz Alp Aksoy, Gizem Öztürk
article en

Abstract

We present a school-aged girl with ataxia-telangiectasia (AT), a rare autosomal recessive neurodegenerative disorder. She presented with progressive cerebellar ataxia beginning at 12 months, ocular telangiectasias developing at 4 years and unusually extensive cutaneous telangiectasias on the dorsum of hands, feet and limbs emerging at 5 years. Laboratory investigations revealed elevated alpha-fetoprotein levels, decreased immunoglobulin A and G and cerebellar atrophy on MRI. The patient experienced recurrent sinopulmonary infections requiring monthly intravenous immunoglobulin therapy. This patient demonstrates the classical neurological manifestations of AT alongside an atypical distribution of prominent cutaneous telangiectasias, emphasising the importance of early recognition for appropriate management and genetic counselling.

BMJ Case ReportsVol. 18(12)
Izmir University (TR), Royal North Shore Hospital (AU), Centenary Institute (AU), Izmir Tepecik Eğitim ve Araştırma Hastanesi (TR)
Gender equality
Openalex Percentile: Top 35%
DNA Repair Mechanisms
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Progressive cerebellar ataxia with extensive peripheral telangiectasias in ataxia-telangiectasia — Yagiz Alp Aksoy, Gizem Öztürk · BMJ Case Reports (2025) | TGRS Research Map | TGRS