The Keutel syndrome

Author:

Ziereisen F.,De Munter C.,Perlmutter N.

Publisher

Springer Science and Business Media LLC

Subject

Radiology, Nuclear Medicine and imaging,Pediatrics, Perinatology and Child Health

Reference8 articles.

1. Keutel J (1972) A new autosomal recessive syndrome: peripheral pulmonary stenosis, brachytelephalangism, neural hearing loss and abnormal cartilage calcification/ossification. In: Bergsma D, Lenz W (eds) The cardiovascular system. Liss (for the National Foundation-March of Dimes), New York, pp 60–68

2. Say B, Balci S, Pirnar T, Israel R, Atasu N (1973) Unusual calcium deposition in cartilage associated with short stature and peculiar facial features: a case report. Pediatr Radiol 1: 127–129

3. Walbaum R, Boniface L, Tonnel A, Desaulty A, Decroix G (1975) Le syndrome de Keutel. Ann Pediatr (Paris) 51: 461

4. Fryns JP, van Fleteren A, Mattelaer P, van den Berghe H (1984) Calcification of cartilages, brachytelephalangy and peripheral pulmonary stenosis: confirmation of the Keutel syndrome. Eur J Pediatr 142: 201–203

5. Edward J, Cormode MD, Lowry RB (1986) Keutel syndrome: clinical report and literature review. Am J Med Genet 24: 289–294

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1. Auditory Profile of Children With Some Rare Neurodevelopmental Disorders;Research Anthology on Pediatric and Adolescent Medicine;2022

2. Keutel Syndrome, a Review of 50 Years of Literature;Frontiers in Cell and Developmental Biology;2021-04-29

3. Auditory Profile of Children With Some Rare Neurodevelopmental Disorders;Emerging Trends in the Diagnosis and Intervention of Neurodevelopmental Disorders;2019

4. A Novel MGP Gene Mutation Causing Keutel Syndrome in a Brazilian Patient;Molecular Syndromology;2018

5. New perspectives on rare connective tissue calcifying diseases;Current Opinion in Pharmacology;2016-06

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