কক্ষের সংখ্যা হ্রাস কারণে একটি অঙ্গ অনুন্নয়ন

hypoplasia's Usage Examples:

Pontocerebellar hypoplasia (PCH) is a heterogeneous group of rare neurodegenerative disorders caused by genetic mutations and characterised by progressive.

Maxillary hypoplasia, or maxillary deficiency, is an underdevelopment of the bones of the upper jaw.

Enamel hypoplasia is a defect of the teeth in which the enamel is deficient in quantity, caused by defective enamel matrix formation during enamel development.

It is also sometimes called mandibular hypoplasia.

DAX1 (dosage-sensitive sex reversal, adrenal hypoplasia critical region, on chromosome X, gene 1) is a nuclear receptor protein that in humans is encoded.

X-linked adrenal hypoplasia congenita is a genetic disorder that mainly affects males.

Salivary gland hypoplasia is relative underdevelopment of the Salivary glands.

Salivary gland hypoplasia tends to produce xerostomia (dry mouth), with.

FSH in females, also referable to as ovarian follicle hypoplasia or granulosa cell hypoplasia in females, is a rare autosomal recessive genetic and endocrine.

Focal dermal hypoplasia is a form of ectodermal dysplasia.

Leydig cell hypoplasia (or aplasia) (LCH), also known as Leydig cell agenesis, is a rare autosomal recessive genetic and endocrine syndrome affecting an.

Caudal regression syndrome, or sacral agenesis (or hypoplasia of the sacrum), is a rare birth defect.

Enamel hypoplasia manifests in a variety of ways depending on the type of AI an individual.

Optic nerve hypoplasia (ONH) is a medical condition arising from the underdevelopment of the optic nerve(s).

There are a few slightly more common diagnoses such as pulmonary hypoplasia, cryptorchidism, congenital heart defects, tracheoesophageal fistulas.

pulmonary hypoplasia and pulmonary hypertension.

Experts disagree on the relative importance of these two conditions, with some focusing on hypoplasia, others.

Micromastia (also called hypomastia, breast aplasia, breast hypoplasia, or mammary hypoplasia) is a medical term describing the postpubertal underdevelopment.

Thymic hypoplasia is a condition where the thymus is underdeveloped or involuted.

Cartilage–hair hypoplasia (CHH) is a rare genetic disorder.

Cerebellar hypoplasia is characterized by reduced cerebellar volume, even though cerebellar shape is (near) normal.

hypoplasia's Meaning':

underdevelopment of an organ because of a decrease in the number of cells

Synonyms:

dysplasia;

Antonyms:

normality;