Fraser syndrome (cryptophthalmos–syndactyly syndrome) is a rare autosomal recessive
malformation disorder. The first description of the syndrome was reported by George Fraser …

This chapter discusses the spectrum of congenital lung disease from the upper airway down
to the lung parenchyma and microvasculature, and associated relevant malformations in the …

Objectives To examine and compare the outcomes of various surgical interventions for
congenital laryngeal webs in terms of avoidance of tracheostomy, rate of decannulation …

Fraser syndrome is an uncommon autosomal recessive disorder with a wide range of
manifestations, including subglottic stenosis and laryngeal webs. Airway compromise …

Supraglottic stenosis is a rare entity, which is more common in females, and trauma is the
most common cause for it. Dysphagia, dysphonia, dyspnea and stridor are the common …

Fraser syndrome, reported by George Fraser in 1962, is a rare autosomal recessive genetic
disorder with three subdivisions (type 1, 2, and 3)(Fraser 1962). This condition is associated …

Аннотация Fraser синдром (OMIM# 219000; ORPHA: 2052; МКБ-10: Q87. 0)–орфанное
заболевание с аутосомно-рецессивным типом наследования, характеризуется …

Abstract Fraser syndrome (OMIM# 219000; ORPHA: 2052; ICD-10: Q87. 0) is a rare, disease
with an autosomal recessive type of inheritance is characterized by abnormalities in the …

The recommendation to describe what is actually seen should be followed by the clinician
both before and after birth. In principle, antenatal ultrasound abnormalities should be …

Introduction: Fraser syndrome is one of the rare congenital anomalies occurring when
fingers or toes, and eyelid formation fail to separate during pregnancy. The purpose of this …