A novel homozygous AP4B1 mutation in two brothers with AP‐4 deficiency syndrome and ocular anomalies

• Published in: American journal of medical genetics. Part A Vol. 176; no. 4; pp. 985 - 991
• Main Authors: Accogli, Andrea, Hamdan, Fadi F., Poulin, Chantal, Nassif, Christina, Rouleau, Guy A., Michaud, Jacques L., Srour, Myriam
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.04.2018
• Subjects: Adaptor Protein Complex 4 - genetics; Adolescent; AP4B1; AP‐4 complex; AP‐4 deficiency; Atrophy; Brain - abnormalities; cataract; Cataracts; Child; Epilepsy; Eye; Eye Abnormalities - diagnosis; Eye Abnormalities - genetics; Face; Facies; Genetic Association Studies; Homozygote; Horner syndrome; Humans; Innervation; Magnetic Resonance Imaging; Male; Microcephaly; Mutation; Optic nerve; Pedigree; Phenotype; Phenotypes; Severity of Illness Index; Siblings; spastic tetraplegia; Spasticity; Substantia alba; Sympathetic nervous system; Syndrome; AP-4 complex; spastic tetraplegia; cataract; AP-4 deficiency; AP4B1; Horner syndrome
• ISSN: 1552-4825; 1552-4833
• DOI: 10.1002/ajmg.a.38628

Adaptor protein complex‐4 (AP‐4) is a heterotetrameric protein complex which plays a key role in vesicle trafficking in neurons. Mutations in genes affecting different subunits of AP‐4, including AP4B1, AP4E1, AP4S1, and AP4M1, have been recently associated with an autosomal recessive phenotype, consisting of spastic tetraplegia, and intellectual disability (ID). The overlapping clinical picture among individuals carrying mutations in any of these genes has prompted the terms “AP‐4 deficiency syndrome” for this clinically recognizable phenotype. Using whole‐exome sequencing, we identified a novel homozygous mutation (c.991C>T, p.Q331*, NM_006594.4) in AP4B1 in two siblings from a consanguineous Pakistani couple, who presented with severe ID, progressive spastic tetraplegia, epilepsy, and microcephaly. Sanger sequencing confirmed the mutation was homozygous in the siblings and heterozygous in the parents. Similar to previously reported individuals with AP4B1 mutations, brain MRI revealed ventriculomegaly and white matter loss. Interestingly, in addition to the typical facial gestalt reported in other AP‐4 deficiency cases, the older brother presented with congenital left Horner syndrome, bilateral optic nerve atrophy and cataract, which have not been previously reported in this condition. In summary, we report a novel AP4B1 homozygous mutation in two siblings and review the phenotype of AP‐4 deficiency, speculating on a possible role of AP‐4 complex in eye development.