অঙ্গ অথবা কক্ষের অস্বাভাবিক ডেভেলপমেন্ট (

dysplasia's Usage Examples:

Dysplasias on a mainly microscopic scale include epithelial dysplasia and fibrous dysplasia of bone.

categories: nondysplastic, low-grade dysplasia, high-grade dysplasia, and frank carcinoma.

High-grade dysplasia and early stages of adenocarcinoma may.

Cleidocranial dysostosis (CCD), also called cleidocranial dysplasia, is a birth defect that mostly affects the bones and teeth.

Brachydactyly Temtamy type Type A5, BDA5 112900 Brachydactyly type A5 nail dysplasia.

Hip dysplasia is an abnormality of the hip joint where the socket portion does not fully cover the ball portion, resulting in an increased risk for joint.

In dogs, hip dysplasia is an abnormal formation of the hip socket that, in its more severe form, can eventually cause lameness and arthritis of the joints.

Ectodermal dysplasia (ED) is a group of genetic syndromes all deriving from abnormalities of the ectodermal structures.

Dentin dysplasia (DD) is a rare genetic developmental disorder affecting dentine production of the teeth, commonly exhibiting an autosomal dominant inheritance.

The condition is also known as Lewandowsky-Lutz dysplasia, named after the physicians who first documented it, Felix Lewandowsky.

Hypohidrotic ectodermal dysplasia is one of about 150 types of ectodermal dysplasia in humans.

Arrhythmogenic cardiomyopathy (ACM), arrhythmogenic right ventricular dysplasia (ARVD), or arrhythmogenic right ventricular cardiomyopathy (ARVC), is.

Anal dysplasia is a pre-cancerous condition which occurs when the lining of the anal canal undergoes abnormal changes.

severity from temporary lameness due to bone growth whilst young to hip dysplasia or spinal disc herniation.

suspected when two or more of the following features are present: Fibrous dysplasia Hyperpigmented skin lesions with characteristic features, including jagged.

"Rapp–Hodgkin and Hay–Wells ectodermal dysplasia syndromes represent a variable spectrum of the same genetic disorder".

Clouston's hidrotic ectodermal dysplasia is caused by mutations in a connexin gene, GJB6 or connexin-30, characterized by scalp hair that is wiry, brittle.

Fairbank's disease or multiple epiphyseal dysplasia (MED) is a rare genetic disorder (dominant form: 1 in 10,000 births) that affects the growing ends.

syndrome; see Naming) is one of at least 150 known types of ectodermal dysplasia.

Diastrophic dysplasia is an autosomal recessive dysplasia which affects cartilage and bone development.

dysplasia's Meaning':

abnormal development (of organs or cells

Synonyms:

aplasia; abnormality; hyperplasia; fibrous dysplasia of bone; abnormalcy; anaplasia; hypertrophy; hypoplasia;

Antonyms:

normality; typicality; familiarity; status; expectedness;