AbstractBackground and objectivesWalker–Warburg Syndrome is a rare, autosomal recessive congenital muscular dystrophy manifested by central nervous system, eye malformations and possible multisystem involvement. The diagnosis is established by the presence of four criteria: congenital muscular dystrophy, type II lissencephaly, cerebellar malformation, and retinal malformation. Most of the syndromic children die in the first three years of life because of respiratory failure, pneumonia, seizures, hyperthermia and ventricular fibrillation.Case reportThe anesthetic management of a two-months-old male child listed for elective ventriculo-peritoneal shunt operation was discussed.ConclusionsA careful anesthetic management is necessary due to the ...
The purpose of this study is to describe two infants that were diagnosed with Walker-Warburg syndrom...
AbstractBackground and objectivesLeigh syndrome (LS) is a rare disease caused by abnormalities of mi...
Anesthesiafor a child with Menkes syndromePurpose/aim:Menkes syndrome is an X-linked recessively inh...
AbstractBackground and objectivesWalker–Warburg Syndrome is a rare, autosomal recessive congenital m...
WOS: 000337101400011PubMed: 24794457Background and objectives: Walker-Warburg Syndrome is a rare, au...
Background and objectives: Walker–Warburg Syndrome is a rare, autosomal recessive congenital muscula...
Walker–Warburg syndrome is a rare congenital disorder. Several features, including muscular dystroph...
Marinesco-Sjogren syndrome (MSS) is a rare autosomal recessive disorder with different clinical sign...
Dandy–Walker Syndrome (DWS) is a rare congenital brain anomaly affecting the cerebellum and the four...
Walker-Warburg syndrome (WWS) is a rare autosomal recessive congenital muscular dystrophy with brain...
Dandy-Walker Syndrome (DWS) is an intrauterine developmental anomaly, which consists of 4-12 % of al...
Purpose: Walker-Warburg syndrome (WWS) is a type of congenital muscular dystrophy (CMD) characterise...
AbstractA 17year old female patient with a biotinidase enzyme deficiency, cerebral palsy, aphamis, g...
Walker-Warburg syndrome (WWS) is a rare and lethal autosomal recessive disorder, caused by defective...
Rothmund–Thomson syndrome (RTS) or poikiloderma congenitale is a rare autosomal recessive disorder. ...
The purpose of this study is to describe two infants that were diagnosed with Walker-Warburg syndrom...
AbstractBackground and objectivesLeigh syndrome (LS) is a rare disease caused by abnormalities of mi...
Anesthesiafor a child with Menkes syndromePurpose/aim:Menkes syndrome is an X-linked recessively inh...
AbstractBackground and objectivesWalker–Warburg Syndrome is a rare, autosomal recessive congenital m...
WOS: 000337101400011PubMed: 24794457Background and objectives: Walker-Warburg Syndrome is a rare, au...
Background and objectives: Walker–Warburg Syndrome is a rare, autosomal recessive congenital muscula...
Walker–Warburg syndrome is a rare congenital disorder. Several features, including muscular dystroph...
Marinesco-Sjogren syndrome (MSS) is a rare autosomal recessive disorder with different clinical sign...
Dandy–Walker Syndrome (DWS) is a rare congenital brain anomaly affecting the cerebellum and the four...
Walker-Warburg syndrome (WWS) is a rare autosomal recessive congenital muscular dystrophy with brain...
Dandy-Walker Syndrome (DWS) is an intrauterine developmental anomaly, which consists of 4-12 % of al...
Purpose: Walker-Warburg syndrome (WWS) is a type of congenital muscular dystrophy (CMD) characterise...
AbstractA 17year old female patient with a biotinidase enzyme deficiency, cerebral palsy, aphamis, g...
Walker-Warburg syndrome (WWS) is a rare and lethal autosomal recessive disorder, caused by defective...
Rothmund–Thomson syndrome (RTS) or poikiloderma congenitale is a rare autosomal recessive disorder. ...
The purpose of this study is to describe two infants that were diagnosed with Walker-Warburg syndrom...
AbstractBackground and objectivesLeigh syndrome (LS) is a rare disease caused by abnormalities of mi...
Anesthesiafor a child with Menkes syndromePurpose/aim:Menkes syndrome is an X-linked recessively inh...