Bartov syndróm, v literatúre známy aj pod akronymickým názvom CLAS (Congenital Localised Absence of Skin), prvý raz opísal Bart v roku 1966 ako vrodené lokalizované chýbanie kože, epidermolysis bullosa congenita a nechtové abnormity. V príspevku autori prezentujú makroskopický aj histologický nález nekroptického prípadu novorodenca s Bartovým syndrómom, s epidermolysis bullosa junctionalis a s atréziou pyloru, ktorý zomrel po 17 dňoch od narodenia a 13 dňoch od operácie stenózy pyloru.
Bart‘s syndrome, in literature also known under the name CLAS (Congenital Localised Absence of Skin), first described by Bart in 1966 as congenital localized absence of skin, epidermolysis bullosa congenita and nail abnormalities. The authors present a macroscopic and histological findings of a newborn with Bart‘s syndrome, with epidermolysis bullosa junctionalis and atresia pylori, who died 17 days after birth and 13 days after surgery for pyloric stenosis.
- MeSH
- Epidermolysis Bullosa, Junctional * diagnosis genetics pathology MeSH
- Skin Diseases diagnosis pathology MeSH
- Humans MeSH
- Mutation MeSH
- Infant, Newborn MeSH
- Autopsy MeSH
- Cause of Death MeSH
- Pylorus abnormalities pathology MeSH
- Syndrome MeSH
- Congenital Abnormalities MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Infant, Newborn MeSH
- Publication type
- Case Reports MeSH
- MeSH
- Endoscopy MeSH
- Proton Pump Inhibitors MeSH
- Middle Aged MeSH
- Humans MeSH
- Proton Pumps therapeutic use MeSH
- Pylorus abnormalities MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Female MeSH
- Publication type
- Case Reports MeSH
- Congress MeSH
- MeSH
- Adult MeSH
- Gastroscopy MeSH
- Humans MeSH
- Pylorus abnormalities MeSH
- Aged MeSH
- Stomach Ulcer diagnosis drug therapy MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Publication type
- Case Reports MeSH
- MeSH
- Child MeSH
- Esterases analysis blood MeSH
- Fatty Acids metabolism MeSH
- Pylorus abnormalities MeSH
- Check Tag
- Child MeSH
