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laryngomalacia/hluchota
Odkaz je uložen do schránky
Strana 1 z 25 Výsledek
Vici syndrome associated with sensorineural hearing loss and laryngomalacia.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
The phenotypically heterogeneous, autosomal recessive Vici syndrome was first described in 1988 in a sister and brother with oculocutaneous albinism, agenesis of the corpus callosum, cataract, cardiomyopathy, cleft lip, and immunodeficiency. Only 14 cases of Vici syndrome have yet been reported,
Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Familial laryngomalacia in two siblings with syndromic features.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
We present two siblings with severe laryngomalacia requiring surgical intervention during the newborn period, microcephaly, developmental delay, cleft palate, preaxial polydactyly, dysplastic nails and conductive hearing loss (persistent after tympanostomy tube placement). In addition the girl has
Waardenburg syndrome associated with laryngomalacia.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Waardenburg syndrome (WS) is a rare autosomal dominant condition characterised by sensorineural hearing loss, in conjunction with pigmentary abnormalities and defects of the neural crest-derived tissues. Depending on the additional phenotypic characteristics, WS is classified into four types, viz.
Natural course of neonatal progeroid syndrome.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
BACKGROUND
Several progeroid disorders presenting a specific "old-man" appearance since birth or childhood have been described. Here, five patients with a history of severe intrauterine and postnatal growth retardation and pseudohydrocephaloid cranium noted after birth that were suggestive of
A novel sclerosing skeletal dysplasia with mixed sclerosing bone dysplasia, characteristic syndromic features, and clinical and radiographic evidence of male-male transmission.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
We report on a father and his 4-year-old son sharing a characteristic dysmorphic facial phenotype (including hyperteleroism, prominent forehead, and wide nasal bridge), macrocephaly, hearing loss, palatal clefting, developmental delay, hypotonia and bony abnormalities including marked cranial
The prevalence of ear, nose and throat disorders in preschool children with Down's syndrome in Glasgow.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Guidelines suggest that all children with Down's syndrome have hearing testing on a regular basis. Since 2004, the ear, nose and throat (ENT), audiology and education services have conducted a joint clinic for annual ENT health and hearing surveillance of all preschool children with Down's syndrome
Asymmetric phenotype associated with rare myelin protein zero mutation.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Myelin protein zero (MPZ) mutations cause demyelinating neuropathies that range from severe neonatal to milder adult forms. We report a 36-year-old man who developed weakness of his left little finger adduction 3 years earlier. The weakness progressed to his other limbs. Examination revealed mildly
Array-CGH analysis and clinical description of 2q37.3 de novo subtelomeric deletion.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
We report on a 13-year-old girl with normal karyotype and a de novo cryptic terminal deletion of chromosome 2q, detected by subtelomeric FISH analysis. Further investigation with array-CGH analysis using the 1Mb resolution Spectral Chip 2600 (Spectral Genomics) confirmed the deletion and also showed
Genotypic and phenotypic correlations of biotinidase deficiency in the Chinese population.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Biotinidase deficiency is an autosomal recessive disorder that affects the endogenous recycling and release of biotin from dietary protein. This disease was thought to be rare in East Asia. In this report, we delineate the phenotype of biotinidase deficiency in our cohort. The genotypes and
Vici syndrome in siblings born to consanguineous parents.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Vici syndrome (OMIM 242840) is a rare syndrome and since its initial description by Vici et al. [1988], only 29 cases have been reported. We describe two brothers from healthy consanguineous Turkish parents with psychomotor delay, congenital bilateral cataracts, high palate, long philtrum,
The otolaryngologic manifestations of Sotos syndrome.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
OBJECTIVE
Soto's syndrome is a genetic disorder caused by mutations in the NSD1 gene. It is characterized by excessive growth in early life. It features craniofacial abnormalities, developmental delay, hypotonia and advanced bone age. A review of the current literature reveals only chronic otitis
Surgical risk factors in Larsen's syndrome.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
The authors report on a child with typical Larsen's syndrome with some rare findings such as mixed-type hearing loss and with some potentially fatal operative risks including laryngomalacia and cervical instability. A few deaths with Larsen's syndrome have been reported associated with various fatal
Three patients with oculo-auriculo-vertebral spectrum and microdeletion 22q11.2.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
We report on three unrelated patients with the 22q11.2 microdeletion syndrome (del22q11) who have phenotypic anomalies compatible with oculo-auriculo-vertebral spectrum (OAVS). Hemifacial microsomia, unilateral microtia, hearing loss, congenital heart/aortic arch arteries defects, and feeding
[Chromosome 5q-syndrome-ENT pathologies].
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
BACKGROUND
The interstitial deletion of chromosome 5q is a disease of rare incidence, which might be hereditary or caused by spontaneous changes within the chromosome respectively. The pathology is based on the loss of chromosomal material within the long arm of chromosome 5. Clinical manifestations
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