Ethmocephaly
Ethmocephaly is a rare medical condition that affects the development of a baby's face and head. In this article, we'll provide you with a straightforward and easy-to-understand explanation of what ...
Rx Autoimmune, Genetic and Rare Diseases (A – Z)
Median Cleft Face Syndrome
Median Cleft Face Syndrome (MCFS) is a rare medical condition that affects the development of a person's face. In this article, we'll provide you with a simple and clear understanding of MCFS, ...
Macrostomia
Macrostomia is a medical term that describes a condition where a person has a larger-than-normal mouth opening. In this article, we will delve into the types of macrostomia, its potential causes, ...
Microtia
Microtia is a rare condition where a person is born with a smaller or underdeveloped ear. In this article, we'll break down what microtia is, its types, common causes, symptoms, diagnostic tests, ...
Craniofacial Duplication
Craniofacial duplication is a rare congenital condition where a person is born with duplications or abnormalities in the facial and cranial (head) features. In this article, we will break down the ...
Parry-Romberg Syndrome
Parry-Romberg Syndrome, also known as progressive hemifacial atrophy, is a rare condition that primarily affects the skin, muscles, and tissues on one side of the face. While it may not be a widely ...
Apert-Crouzon Syndrome
Apert-Crouzon Syndrome is a rare genetic disorder that affects the development of a person's head and face. This article aims to provide a comprehensive yet simplified explanation of Apert-Crouzon ...
Frontonasal Dysplasia
Frontonasal dysplasia is a condition that affects the development of the face, particularly the nose and forehead. In this article, we'll explore the different types of frontonasal dysplasia, its ...
Hemifacial Microsomia
Hemifacial Microsomia is a rare condition that affects the development of one side of a person's face. In this article, we will explain the different types of Hemifacial Microsomia, explore its ...
Craniofacial Microsomia
Craniofacial Microsomia is a rare medical condition that affects the development of the head and face, leading to various physical abnormalities. In this comprehensive guide, we will break down ...
Goldenhar Syndrome
Goldenhar Syndrome is a rare condition that affects the development of the face and spine. It can vary greatly in its presentation, causing a range of physical and sometimes internal issues. In this ...
Pierre Robin Sequence
Pierre Robin Sequence, often abbreviated as PRS, is a rare congenital condition that affects the development of a baby's face and airway. In simple terms, PRS can cause a baby to be born with a small ...
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