Trisomy 14 mosaicism is a rare chromosome disorder characterized by delayed development, failure to thrive, and facial dysmorphism. Only approximately 30 trisomy 14 mosaicism cases have been reported in the literature because trisomy 14 is associated with early spontaneous abortion. We report a case of a 17-month-old girl with abnormal skin pigmentation, delayed development, facial dysmorphism, and failure to thrive with the 47,XX,+14/46,XX chromosome complement
[[abstract]]Objective: Prenatal diagnosis of mos45,X/46,X,+mar is difficult in genetic counseling. P...
The '13q-' syndrome shows widely variable manifestations. Investigation of the involvement of differ...
Discordance between clinical phenotype and genotype has multiple causes, including mosaicism. Phenot...
Background: Both maternal uniparental disomy 14 (UPD(14)mat) and mosaic trisomy 14 are rare events i...
Postnatally ascertained trisomy 16 mosaicism is a rare diagnosis, with only three reported cases to ...
Background: Trisomy 22 mosaicism is a rare autosomal anomaly with survival compatibility. Recognitio...
Trisomy 4 mosaicism in liveborns is very rare. We describe a 17-month-old girl with trisomy 4 mosaic...
Introduction: Hypomelanosis of Ito is a rare neurocutaneous disorder, characterized by streaks and s...
Background: Mosaic whole-chromosome tetrasomy has not previously been described as a cause of fetal ...
Proximal duplications of chromosome 1q are rare chromosomal abnormalities. Most patients with this c...
Parental mosaicism for trisomy-21 is a recognized reason for the birth of mongol children, and the p...
Complete Trisomy 13 or Patau’s Syndrome is a relatively common (1/10,000 births) and uniformly fatal...
We report on an infant with a multiple congenital anomaly syndrome and severe developmental delay in...
We report on the case of a patient with mosaic trisomy 22, who was diagnosed prenatally by amniocent...
Trisomy 13, or Patau syndrome, is a rare chromosomal disorder characterized by a triad of cleft lip ...
[[abstract]]Objective: Prenatal diagnosis of mos45,X/46,X,+mar is difficult in genetic counseling. P...
The '13q-' syndrome shows widely variable manifestations. Investigation of the involvement of differ...
Discordance between clinical phenotype and genotype has multiple causes, including mosaicism. Phenot...
Background: Both maternal uniparental disomy 14 (UPD(14)mat) and mosaic trisomy 14 are rare events i...
Postnatally ascertained trisomy 16 mosaicism is a rare diagnosis, with only three reported cases to ...
Background: Trisomy 22 mosaicism is a rare autosomal anomaly with survival compatibility. Recognitio...
Trisomy 4 mosaicism in liveborns is very rare. We describe a 17-month-old girl with trisomy 4 mosaic...
Introduction: Hypomelanosis of Ito is a rare neurocutaneous disorder, characterized by streaks and s...
Background: Mosaic whole-chromosome tetrasomy has not previously been described as a cause of fetal ...
Proximal duplications of chromosome 1q are rare chromosomal abnormalities. Most patients with this c...
Parental mosaicism for trisomy-21 is a recognized reason for the birth of mongol children, and the p...
Complete Trisomy 13 or Patau’s Syndrome is a relatively common (1/10,000 births) and uniformly fatal...
We report on an infant with a multiple congenital anomaly syndrome and severe developmental delay in...
We report on the case of a patient with mosaic trisomy 22, who was diagnosed prenatally by amniocent...
Trisomy 13, or Patau syndrome, is a rare chromosomal disorder characterized by a triad of cleft lip ...
[[abstract]]Objective: Prenatal diagnosis of mos45,X/46,X,+mar is difficult in genetic counseling. P...
The '13q-' syndrome shows widely variable manifestations. Investigation of the involvement of differ...
Discordance between clinical phenotype and genotype has multiple causes, including mosaicism. Phenot...