dysostosis multiplex

(redirected from dysostosis)
Also found in: Dictionary, Medical, Encyclopedia, Wikipedia.
Graphic Thesaurus  🔍
Display ON
Animation ON
Legend
Synonym
Antonym
Related
  • noun

Synonyms for dysostosis multiplex

hereditary disease (autosomal recessive) consisting of an error is mucopolysaccharide metabolism

References in periodicals archive ?
This article describes two cases of nonsevere craniofacial dysostosis in a father and son, which were characterized by mesocephaly and ptosis.
The second form, called spondylothoracic dysostosis, also has an autosomal recessive pattern of inheritance and is characterized radiographically by fusion and/or absence of ribs and multiple segmentation defects involving all vertebral levels.
Scapulo-iliac dysostosis (pelvis-shoulder dysplasia, Kosenow syndrome) is an uncommon hereditary skeletal dysplasia.
org 1,2,9; Spanish/Italian materials MANDIBULOFACIAL DYSOSTOSIS See: Nager & Miller Syndromes; Treacher Collins Syndrome MANNOSIDOSIS See: Tay-Sachs Disease MAPLE SYRUP URINE DISEASE See also: Acidemia, Organic; Metabolic Disorders Maple Syrup Urine Disease Family Support Group 5720 Buckfield Ct.
org 9; provides physicians with summaries of consenting, registered patients' anesthesia histories MANDIBULOFACIAL DYSOSTOSIS See: Nager & Miller Syndromes; Treacher Collins Syndrome MANNOSIDOSIS See: Tay-Sachs Disease MAPLE SYRUP URINE DISEASE See also: Acidemia, Organic; Metabolic Disorders Maple Syrup Urine Disease Family Support Group 5720 Buckfield Ct.
net 9; provides physicians with summaries of consenting, registered patients' anesthesia histories MANDIBULOFACIAL DYSOSTOSIS See also Nager & Miller Syndromes; Treacher Collins Syndrome MANNOSIDOSIS See also Tay-Sachs Disease MAPLE SYRUP URINE DISEASE See also: Acidemia, Organic; Metabolic Disorders Maple Syrup Urine Disease Family Support Group 24806 State Rd.
Absence of the mastoid antrum previously has been reported in congenital syndromes such as trisomy 13 and mandibulofacial dysostosis (Treacher Collins syndrome).
2,6) Clinical manifestations of ML III include moderate to severe dysostosis multiplex, stiffness of fingers and shoulders, carpal and tarsal tunnel syndromes, claw-hand deformity, short stature, and scoliosis.
Hypo-hyperdontia is rare in isolation and has been associated with over 50 syndromes, notably orodigitofacial dysostosis, Hallerman Streiff, cleidocranial dysplasia syndrome, Ellis van Creveld, Down syndrome, cleft lip and palate, and many others [Zhu et al.