Abnormality of the nares

Brachycephalic airway syndrome in dogs is typified by a variety of anatomical abnormalities causing a diverse spectrum of… Expand

Pitt-Hopkins syndrome is an emerging neurodevelopmental disorder caused by haploinsufficiency of the TCF4 gene on chromosome… Expand

BACKGROUND Forkhead box G1 gene (FOXG1) mutations and deletions are associated with a congenital variant of Rett syndrome (RTT… Expand

Cold‐induced sweating syndrome (CISS) is a rare autosomal recessive disorder caused by mutations in CRLF1 (cytokine receptor‐like… Expand

We report a brother and sister born to consanguineous parents. The siblings have hypertelorism, bifid nose, upturned nares… Expand

S ubmicroscopic deletion del(9)(q34.3) is a rare constitutional microdeletion syndrome involving the gene-rich subtelomeric… Expand

We report a case with Robinow syndrome which has been rarely reported in the literature. A male newborn who had fetal face… Expand

Patients who are unable to eat by mouth can be fed in a manner that maintains the structural and functional integrity of the… Expand

Editor—Duplication of proximal segments of the long arm of chromosome 10 is rare and results in a pattern of malformations and… Expand

Abstract The technique described produces inrolling and narrowing of the alar base by a predetermined amount, depending upon the… Expand