Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1989 2
1997 1
1999 1
2011 1
2013 1
2017 1
2023 0

Text availability

Article attribute

Article type

Publication date

Search Results

7 results

Results by year

Filters applied: . Clear all
Page 1
Laryngo-tracheo-oesophageal clefts.
Leboulanger N, Garabédian EN. Leboulanger N, et al. Orphanet J Rare Dis. 2011 Dec 7;6:81. doi: 10.1186/1750-1172-6-81. Orphanet J Rare Dis. 2011. PMID: 22151899 Free PMC article. Review.
Depending on the severity of the malformation, patients may present with stridor, hoarse cry, swallowing difficulties, aspirations, cough, dyspnea and cyanosis through to early respiratory distress. ...
Depending on the severity of the malformation, patients may present with stridor, hoarse cry, swallowing difficulties, aspirat …
Vocal cord paralysis.
Grundfast KM, Harley E. Grundfast KM, et al. Otolaryngol Clin North Am. 1989 Jun;22(3):569-97. Otolaryngol Clin North Am. 1989. PMID: 2657584 Review.
Suspect unilateral vocal cord paresis or paralysis in an infant or child with hoarse voice, low-pitched cry, or breathy cry or voice. The infant who develops mild stridor and hoarse cry following surgical repair of a patent ductus arteriosus or …
Suspect unilateral vocal cord paresis or paralysis in an infant or child with hoarse voice, low-pitched cry, or breathy cry …
Vallecular cysts in newborns and young infants.
Gutiérrez JP, Berkowitz RG, Robertson CF. Gutiérrez JP, et al. Pediatr Pulmonol. 1999 Apr;27(4):282-5. doi: 10.1002/(sici)1099-0496(199904)27:4<282::aid-ppul10>3.0.co;2-g. Pediatr Pulmonol. 1999. PMID: 10230929 Review.
Failure to thrive was present in five patients diagnosed later than the first week of life. An abnormal or a hoarse cry was present in only two patients. Diagnosis in all cases was made by endoscopy. ...
Failure to thrive was present in five patients diagnosed later than the first week of life. An abnormal or a hoarse cry was pr …
Congenital hypothyroidism: recommendations of the Thyroid Department of the Brazilian Society of Endocrinology and Metabolism.
Maciel LM, Kimura ET, Nogueira CR, Mazeto GM, Magalhães PK, Nascimento ML, Nesi-França S, Vieira SE; Brazilian Society of Endocrinology and Metabolism. Maciel LM, et al. Arq Bras Endocrinol Metabol. 2013 Apr;57(3):184-92. doi: 10.1590/s0004-27302013000300004. Arq Bras Endocrinol Metabol. 2013. PMID: 23681264 English, Portuguese.
The most frequent symptoms and signs are prolonged neonatal jaundice, hoarse cry, lethargy, slow movements, constipation, macroglossia, umbilical hernia, large fontanelle, hypotonia and dry skin. ...
The most frequent symptoms and signs are prolonged neonatal jaundice, hoarse cry, lethargy, slow movements, constipation, macr …
[A case report of childhood Farber's disease and literature review].
Bao XH, Tian JM, Ji TY, Chang XZ. Bao XH, et al. Zhonghua Er Ke Za Zhi. 2017 Jan 2;55(1):54-58. doi: 10.3760/cma.j.issn.0578-1310.2017.01.011. Zhonghua Er Ke Za Zhi. 2017. PMID: 28072961 Review. Chinese.
Result: The girl, 2 years 2 months old, was sent to our hospital in October 2015, with complains of "joint swelling for 17 months, development regress of intelligence and movement for 11 months, intermittent seizures for 2 months" .The clinical manifestation of the patient was ch …
Result: The girl, 2 years 2 months old, was sent to our hospital in October 2015, with complains of "joint swelling for 17 months, developme …
[Weaver syndrome. 1st case reported in Venezuela].
Sánchez O, Boufajreldin S, Oranges C, Orta C, Guerra D. Sánchez O, et al. Invest Clin. 1997 Mar;38(1):9-24. Invest Clin. 1997. PMID: 9235073 Review. Spanish.
The proband presents persistent pre and post-natal overgrowth, asynchronic advanced bone age, particular facies, (macrocephaly, ocular hypertelorism, micrognathia, large ears), bilateral widening of the distal femoral metaphysis, bilateral tibia vara, prominent fetal fingerpads, …
The proband presents persistent pre and post-natal overgrowth, asynchronic advanced bone age, particular facies, (macrocephaly, ocular hyper …
G syndrome and its otolaryngologic manifestations.
Howell L, Smith JD. Howell L, et al. Ann Otol Rhinol Laryngol. 1989 Mar;98(3):185-90. doi: 10.1177/000348948909800304. Ann Otol Rhinol Laryngol. 1989. PMID: 2647017 Review.
G syndrome is a familial constellation of congenital anomalies that include a distinctive facies, ocular hypertelorism, prominent occiput and forehead, short lingual frenulum, stridor, hoarse cry, and laryngotracheoesophageal (LTE) clefts, as well as hypospadias and …
G syndrome is a familial constellation of congenital anomalies that include a distinctive facies, ocular hypertelorism, prominent occiput an …