Two new patients with focal dermal hypoplasia: A novel PORCN variant and insights on the diagnostic considerations. (3rd January 2022)

• Record Type: Journal Article
• Authors: Elhossini, Rasha Moheb; Abdel‐Hamid, Mohamed S.; Ashaat, Engy; Otaify, Ghada A.; Dawoud, Heba; Elshimy, Khalid; El Ruby, Mona; Aglan, Mona
• Is Part Of: Congenital anomalies. Volume 62:Number 2(2022)
• Page Start: 68
• Page End: 77
• Publication Date: 2022-01-03
• Subjects: bladder extrophy -- focal dermal hypoplasia -- PORCN gene -- skeletal malformations -- skin lesions; Abnormalities, Human -- Periodicals; 616.043
• DOI: 10.1111/cga.12457
• Languages: English
• ISSNs: 0914-3505

Abstract

Abstract: Mutations in the PORCN gene cause an X‐linked dominant condition; focal dermal hypoplasia (FDH), characterized by atrophic skin, pigmented skin lesions in addition to several ocular and skeletal malformations. FDH is rare with around 275 cases reported so far from diverse ethnic groups. Herein, we provide a report of two new patients with FDH from Egypt. In addition to the typical clinical manifestations of the disease, infrequently reported clinical findings in the form of broad metaphysis, bilateral short broad femurs, and dermal sinus over the sacrum were seen in Patient 1 and partial fusion of labia majora, ventral hernia, and bladder extrophy were present in Patient 2. Two heterozygous protein‐truncating PORCN mutations were identified in our patients, a known nonsense c.370C>T p.(Arg124Ter) and a novel frameshift c.375delG p.(Ala126HisfsTer3). Segregation analyses confirmed that the two mutations were "de novo" and not inherited from any of the parents. Our study expands the clinical and mutational spectrum of focal dermal hypoplasia and emphasizes the importance of investigating the different body systems and organs for the early management of patients.