Commentary: Case report: Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP) presenting with liver cirrhosis and steroid-responsive interstitial pneumonia

• Filippo M. Panfili,
• Andrea Pietrobattista,
• Davide Vecchio,
• Michaela V. Gonfiantini,
• Andrea Bartuli,
• Marina Macchiaiolo

Affiliations

Filippo M. Panfili

Rare Diseases and Medical Genetics Unit, Bambino Gesù Children’s Hospital, IRCSS, Rome, Italy

Andrea Pietrobattista

Division of Gastroenterology, Hepatology and Nutrition, Bambino Gesù Children’s Hospital IRCCS, Rome, Italy

Davide Vecchio

Rare Diseases and Medical Genetics Unit, Bambino Gesù Children’s Hospital, IRCSS, Rome, Italy

Michaela V. Gonfiantini

Rare Diseases and Medical Genetics Unit, Bambino Gesù Children’s Hospital, IRCSS, Rome, Italy

Andrea Bartuli

Rare Diseases and Medical Genetics Unit, Bambino Gesù Children’s Hospital, IRCSS, Rome, Italy

Marina Macchiaiolo

Rare Diseases and Medical Genetics Unit, Bambino Gesù Children’s Hospital, IRCSS, Rome, Italy