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Keutel syndrome (KS) is a rare
autosomal recessive genetic disorder characterized by
abnormal diffuse cartilage calcification,
hypoplasia of the mid-face...
- in one or more epiphyses. It is seen in
chondrodysplasia punctata and in
Keutel syndrome. It is also
caused by use of warfarin, alcohol, and in hypothyroidism...
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Vitamin K hydroquinone.
Abnormalities in the MGP gene have been
linked with
Keutel syndrome, a rare
condition characterised by
abnormal calcium deposition...
- MGP
exhibit calcification of
arteries and
other soft tissues. In humans,
Keutel syndrome is a rare
recessive genetic disorder ****ociated with abnormalities...
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Keratosis pilaris Keratosis,
seborrheic Kerion celsi Kernicterus Keutel syndrome Ki-1cell
lymphoma KID
syndrome Kifafa seizure disorder Kikuchi...
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linearis with
ichthyosis congenita and
sclerosing keratoderma syndrome Keutel syndrome Khyâl cap Kimmelstiel-Wilson
syndrome Kindler syndrome King–Kopetzky...
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syndrome Other names Cleft lip/palate-facial, eye,
heart and
intestinal anomalies syndrome Keutel syndrome has an
autosomal recessive pattern of inheritance....
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United States, and no
greater than 1 per 2,000 in Europe. It is
similar to
Keutel, Muenke,
Rubinstein and Teunissen–Cremers syndrome.
Nasodigitoacoustic syndrome...
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inflammatory conditions,
hypervitaminosis D and rare
genetic disorders, such as
Keutel syndrome. The
prevalence of Mönckeberg's
arteriosclerosis in the general...
- doi:10.1128/AM.18.3.406-409.1969. ISSN 0003-6919. PMC 377994. PMID 5373676.
Keutel, J.; Möckel, H. (1
December 1969). "Induction of
chromosomal breakage in...
