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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Thyroid involvement in Chanarin-Dorfman syndrome in adults in the largest series of patients carrying the same founder mutation in ABHD5 gene

Fig. 1

Distribution of clinical, radiological data of patients for each analysis. Abdominal ultrasonography liver (Abd us liver), Abdominal ultrasonography kidney (Abd us kidney), Thyroid Stimulating Hormone (TSH), Free Thyroxine (FT4), Aspartate Transaminase (ASAT), Alanine Transaminase (ALAT), Creatine Phosphokinase (CPK), Magnetic Resonance Imaging (MRI)

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172