Yazarlar |
Özet |
DOI: 10.26650/experimed.2018.431791According to the literature on cases of toe walking, neural tube defects generally refer to orthopedic and neurologic case reports. The case of toe walking has been selected to present the information obtained from our patient group monitored for 6 years and to draw attention to Methylene Tetra Hydro Folate Reductase (MTHFR) polymorphisms. A 10 year-old female patient has was applied for toe walking and mild neurologic retardation. Her family history was unremarkable, except for family history of stroke in her grandfather. Her prominent clinical findings were obesity, sacral dimple and toe walking. The laboratory assessment showed that moderately high lipid levels and MTHFR A1298C heterozygote mutation. A hypoplasic disc, spondylolisthesis and filar lipoma were detected in a spinal MRI. The final diagnoses of 20/8000 patients (11 female, 9 male) monitored in our clinic due to the symptoms of toe walking were as follows: 3 late diagnosed phenylketonuria (PKU), 2 metachromatic leuko-dystrophy (MLD), 1L (OH) glutaric aciduria, 3fatty acids oxidation defect (FAO), 1 mitochondrial disease and 10 MTHFR. A problem was detected in medium chain fatty acids in the patients with FAO. The complaint was considered to be muscle cramp due to increased muscle enzymes and aches throughout the complaint period. Considering neurological findings, the difficulties in walking were apparent in PKU and MLD patients. A short Achilles tendon was included in neurological findings in the patients diagnosed with L2 glutaric aciduria and mitochondrial diseases. From MTHFR patients, syringomyelia was found ... |
Anahtar Kelimeler |
Makale Türü | Özgün Makale |
Makale Alt Türü | Uluslararası alan indekslerindeki dergilerde yayımlanan tam makale |
Dergi Adı | Deneysel Tıp Araştırma Enstitüsü Dergisi |
Dergi Tarandığı Indeksler | |
Makale Dili | İngilizce |
Basım Tarihi | 09-2018 |
Cilt No | 81 |
Sayı | 1 |
Sayfalar | 37 / 40 |
Doi Numarası | 10.26650/experimed.2018.431791 |