ABSTRACTWe report the case of a patient with Patau syndrome, diagnosed by skin karyotype, emphasizing the applications and importance of this test. The pregnancy morphology ultrasound showed face defects and of central nervous system and heart chambers asymmetry. In the postnatal evaluation it was identified microcephaly, single central nostril, and other malformations. We performed skin karyotype that resulted in full trisomy 13. Our report highlights the possibility of performing karyotype examination in cases when it is no longer possible to obtain a blood sample, thus providing the correct diagnosis and genetic counseling for the family
Abstract Background Trisomy 13 or Patau syndrome has a prevalence of 1:10,000–20,000 and is characte...
Tato bakalářská práce je věnována syndromu s názvem Patauův. Řadí se mezi genetická onemocnění, kter...
Background: Trisomy 13 is a trisomy disorder of chromosome 13 which causes many fetal structural def...
In recent years, prenatal diagnosis and elective pregnancy termination have affected the reported bi...
A cytogenetic re-evaluation at 9 years of age brought to light in skin fibroblasts a third cell line...
We report a 12-year-old patient with Patau syndrome, in whom two cell lines were present from birth,...
Patau syndrome is the least common and most severe of the viable autosomal trisomies with median sur...
OBJECTIVE: To describe gestational, perinatal and family findings of patients with Patau syndrome (P...
Patau syndrome is associated with extra chromosome 13 material, either free as in the 47,+13 or in a...
Trisomy 13 (Patau syndrome) is cytogenetically classified as a 47,XY,+13 or 47,XX,+13, due to nondis...
Trisomy 13, or Patau syndrome, is a rare chromosomal disorder characterized by a triad of cleft lip ...
Patau syndrome when caused by attachment of an extra chromosome with chromosome 13 is called as full...
Trisomi 13 (sindrom Patau) merupakan kelainan kromosom yang ditandai dengan ekstra duplikasi kromoso...
Holoprosencephaly (HPE) is a congenital defect of the brain, median structures, and face resulting f...
ABSTRACTA case of D1 trisomy is reported. The patient suffered of multiple congenital anomalies, whi...
Abstract Background Trisomy 13 or Patau syndrome has a prevalence of 1:10,000–20,000 and is characte...
Tato bakalářská práce je věnována syndromu s názvem Patauův. Řadí se mezi genetická onemocnění, kter...
Background: Trisomy 13 is a trisomy disorder of chromosome 13 which causes many fetal structural def...
In recent years, prenatal diagnosis and elective pregnancy termination have affected the reported bi...
A cytogenetic re-evaluation at 9 years of age brought to light in skin fibroblasts a third cell line...
We report a 12-year-old patient with Patau syndrome, in whom two cell lines were present from birth,...
Patau syndrome is the least common and most severe of the viable autosomal trisomies with median sur...
OBJECTIVE: To describe gestational, perinatal and family findings of patients with Patau syndrome (P...
Patau syndrome is associated with extra chromosome 13 material, either free as in the 47,+13 or in a...
Trisomy 13 (Patau syndrome) is cytogenetically classified as a 47,XY,+13 or 47,XX,+13, due to nondis...
Trisomy 13, or Patau syndrome, is a rare chromosomal disorder characterized by a triad of cleft lip ...
Patau syndrome when caused by attachment of an extra chromosome with chromosome 13 is called as full...
Trisomi 13 (sindrom Patau) merupakan kelainan kromosom yang ditandai dengan ekstra duplikasi kromoso...
Holoprosencephaly (HPE) is a congenital defect of the brain, median structures, and face resulting f...
ABSTRACTA case of D1 trisomy is reported. The patient suffered of multiple congenital anomalies, whi...
Abstract Background Trisomy 13 or Patau syndrome has a prevalence of 1:10,000–20,000 and is characte...
Tato bakalářská práce je věnována syndromu s názvem Patauův. Řadí se mezi genetická onemocnění, kter...
Background: Trisomy 13 is a trisomy disorder of chromosome 13 which causes many fetal structural def...