Novel CRLF1 gene mutation in a newborn infant diagnosed with Crisponi syndrome |
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Authors: | Nilay Hakan Fatma Tuba Eminoglu Mustafa Aydin Aysegul Zenciroglu Nazmiye Nilgun Karadag Arzu Dursun Nurullah Okumus Serdar Ceylaner |
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Affiliation: | 1. Departments of Neonatology;2. Nutrition and Metabolism, Dr. Sami Ulus Maternity and Children Training and Research Hospital;3. Intergen Genetic Disease Diagnostic Center, Ankara, Turkey |
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Abstract: | Crisponi syndrome is an infrequently described disorder with autosomal recessive trait. It is characterized by extensive muscular contractions in the face after even minimal stimuli or crying, hypertonia, opisthotonus, camptodactyly, and typical facial features. Muscle contractions attenuate during rest or when the infant calms down. As a recently described new disease, Crisponi syndrome may be confused with epileptic manifestations. Most of the patients die in the first months of life due to hyperthermia and feeding problems. Recently, it has been demonstrated that mutations of the CRLF1 gene ‘cytokine receptor‐like factor 1’ are associated with Crisponi syndrome. Here, we present a newborn diagnosed with Crisponi syndrome and report a novel homozygous CFRL1 gene mutation. |
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Keywords: | camptodactyly Crisponi syndrome CRLF1 gene hypertonia mutation |
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