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Understanding Polysyndactyly Overgrowth Syndrome
Introduction to Polysyndactyly Overgrowth Syndrome Disease⁚ Polysyndactyly Overgrowth Syndrome The Polysyndactyly Overgrowth Syndrome is a […]
Understanding Porphyria Cutanea Tarda, Familial Type: Causes, Symptoms, Diagnosis, and Treatment
Introduction Porphyria Cutanea Tarda, Familial Type, is a rare inherited disorder causing skin blisters, hair […]
Understanding Popliteal Pterygium Syndrome: Causes, Genetics, Clinical Features, and Epidemiology
Article Plan⁚ Disease — Popliteal Pterygium Syndrome Overview of Popliteal Pterygium Syndrome Popliteal pterygium syndrome […]
Understanding Pontocerebellar Hypoplasia: Symptoms, Genetics, and Diagnosis
Introduction to Pontocerebellar Hypoplasia Pontocerebellar Hypoplasia (PCH) is a rare group of neurodegenerative disorders characterized […]
Overview of Porencephaly-Cerebellar Hypoplasia-Internal Malformations Syndrome
Introduction to Porencephaly-Cerebellar Hypoplasia-Internal Malformations Syndrome Porencephaly-cerebellar hypoplasia-internal malformations syndrome is rare central nervous system […]
Overview of Popliteal Pterygium Syndrome Lethal Type
Autosomal recessive multiple pterygium syndrome (MPS) is a rare disorder associated with anomalies affecting skin, […]
Porencephaly⁚ An Overview of a Rare Congenital Disorder
Introduction to Porencephaly Porencephaly is an extremely rare congenital disorder of the central nervous system […]
Understanding Lymphomatoid Papulosis (LyP): Symptoms, Diagnosis, and Management
Disease ‒ LyP (Lymphomatoid Papulosis) Introduction to LyP Lymphomatoid Papulosis (LyP) is a rare skin […]
Understanding Lyngstadaas Syndrome: A Comprehensive Guide
Understanding Lyngstadaas Syndrome Lyngstadaas syndrome is a rare genetic disorder with unique characteristics․ This article […]