Novel progressive acrodysostosis-like skeletal dysplasia, cerebellar atrophy, and ichthyosis.

Abstract

Acrodysostosis refers to a rare heterogeneous group of bone dysplasias that share skeletal features, hormone resistance, and intellectual disability. Two genes have been associated with acrodysostosis with or without hormone resistance (PRKAR1A and PDE4D). Severe intellectual disability has been reported with acrodysostosis but brain malformations and ichthyosis have not been reported in these syndromes. Here we describe a female patient with acrodysostosis, intellectual disability, cerebellar hypoplasia, and lamellar ichthyosis. The patient has an evolving distinctive facial phenotype and childhood onset ataxia. X-rays showed generalized osteopenia, shortening of middle and distal phalanges, and abnormal distal epiphysis of the ulna and radius. Brain magnetic resonance imaging showed cerebellar atrophy without other brainstem abnormalities. Genetic workup included nondiagnostic chromosomal microarray and skeletal dysplasia molecular panels. These clinical findings are different from any recognized form of acrodysostosis syndrome. Whole exome sequencing did not identify rare or predicted pathogenic variants in genes associated with known acrodysostosis, lamellar ichthyosis, and other overlapping disorders. A broader search for rare alleles absent in healthy population databases and controls identified two heterozygous truncating alleles in FBNL7 and PPM1M genes, and one missense allele in the NPEPPS gene. Identification of additional patients is required to delineate the mechanism of this unique disorder.

• Authors: Harvy M Velasco, Ehsan Ullah, Angela M Martin, Robert B Hufnagel, Carlos E Prada
• Journal: American journal of medical genetics. Part A (Am J Med Genet A) Vol. 182 Issue 10 Pg. 2214-2221 (10 2020) ISSN: 1552-4833 [Electronic] United States
• PMID: 32783359 (Publication Type: Case Reports, Journal Article, Research Support, N.I.H., Intramural)
• Copyright: © 2020 Wiley Periodicals LLC.

Chemical References

• Calcium-Binding Proteins
• FBLN7 protein, human
• PPM1M protein, human
• Phosphoprotein Phosphatases

Topics

• Adolescent
• Adult
• Atrophy (complications, diagnosis, genetics, pathology)
• Calcium-Binding Proteins (genetics)
• Cerebellum (abnormalities, pathology)
• Child
• Child, Preschool
• Developmental Disabilities (complications, diagnosis, genetics, pathology)
• Dysostoses (complications, diagnosis, genetics, pathology)
• Epiphyses (physiopathology)
• Female
• Heterozygote
• Humans
• Ichthyosis (complications, diagnosis, genetics, pathology)
• Intellectual Disability (complications, diagnosis, genetics, pathology)
• Middle Aged
• Musculoskeletal Abnormalities (genetics, physiopathology)
• Mutation, Missense (genetics)
• Nervous System Malformations (complications, diagnosis, genetics, pathology)
• Osteochondrodysplasias (complications, diagnosis, genetics, pathology)
• Phosphoprotein Phosphatases (genetics)
• Exome Sequencing
• Young Adult