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Congenital abnormality of a small prostate gland
Prostate hypoplasia is the congenital abnormality of a small (or absent) prostate gland. Often associated with other abnormalities of the urogenital system
Prostate_hypoplasia
Medical condition
cell hypoplasia, anti-Müllerian hormone is secreted normally and so there are no Müllerian structures. Wolffian structures, such as the prostate, vasa
Leydig_cell_hypoplasia
Medical condition
ejaculatory ducts) are normal but testes are usually undescended and prostate hypoplasia is common. Males with the same mutations in SRD5A2 can have different
5α-Reductase_2_deficiency
Pair of simple tubular glands
include failure to develop, either completely (agenesis) or partially (hypoplasia), and cysts. Failure of the vesicles to form is often associated with
Seminal_vesicles
Type of hormone therapy
feminization and suppress androgens Breast hypoplasia or as a means of hormonal breast enhancement in women Uterine hypoplasia in women Premenstrual syndrome and
High-dose_estrogen_therapy
Patel–Bixler syndrome Patella aplasia, coxa vara, tarsal synostosis Patella hypoplasia mental retardation Patellofemoral pain syndrome Patent ductus arteriosus
List_of_diseases_(P)
Chemical compound
others, is an estrogen medication which has been used in the treatment of prostate cancer in men. It has also been used as a part of hormone therapy for transgender
Estradiol_undecylate
Chemical compound
deficiency, treatment of prostate cancer and breast cancer, and other uses. By 2007, it was only used in the treatment of prostate cancer and breast cancer
Diethylstilbestrol
Enlargement of tissue due to cell proliferation
conditions leading to hyperplasia, include: Benign prostatic hyperplasia, also known as prostate enlargement. Cushing's disease – Physiopathology of
Hyperplasia
Diminished activity of the gonads
Examples of pituitary defects include hypopituitarism and pituitary hypoplasia. An example of hypogonadism resulting from the lack of hormone response
Hypogonadism
Growth of fibrous or connective tissue
carcinoma Cutaneous leiomyosarcoma Cutaneous metastasis The stroma of the prostate is characteristically muscular. Due to this muscularity, detecting the
Desmoplasia
Medical condition
lead to the Potter sequence of atypical physical appearance. Pulmonary hypoplasia is by far the main cause of death in the early neonatal period for children
Urinary_tract_obstruction
Excess urea in the blood due to kidney dysfunction
generalized immunosuppression. In children with renal disease, enamel hypoplasia of the primary and permanent dentition has been observed. The abnormalities
Uremia
Normal or spontaneous enlargement of breasts
transgender women, as well as hormonal breast enhancement in women with breast hypoplasia or small breasts, mammoplasia is a desired effect. Breast atrophy – Shrinkage
Mammoplasia
intrahepatic, syndromic form Biliary atresia Biliary cirrhosis Biliary hypoplasia Biliary malformation renal tubular insufficiency Biliary tract cancer
List_of_diseases_(B)
Medication producing effects similar to progesterone
endometrial hyperplasia, endometriosis, uterine fibroids, and uterine hypoplasia. Progestogens are used to treat benign breast disorders. They are associated
Progestogen_(medication)
studied in the treatment of prostate cancer in men. Intrauterine estradiol has been studied in the treatment of uterine hypoplasia in women. The administration
Pharmacokinetics_of_estradiol
Syndromes
antagonist-associated Churg–Strauss syndrome Levator ani syndrome Leydig cell hypoplasia Liddle's syndrome Liebenberg syndrome LIG4 syndrome Lima syndrome Limb
List_of_syndromes
Medical condition
of germ cell malignancy to be as low as 0.8% before puberty. Vaginal hypoplasia, a relatively frequent finding in CAIS and some forms of PAIS, is associated
Complete androgen insensitivity syndrome
Complete_androgen_insensitivity_syndrome
Medical condition
receptors) – carbohydrate-deficient glycoprotein syndrome, Leydig cell hypoplasia (or insensitivity to LH) in males, FSH insensitivity in females, and LH
Hypergonadotropic hypogonadism
Hypergonadotropic_hypogonadism
Protein-coding gene in the species Homo sapiens
that EN2 could be a marker for prostate cancer which might prove more reliable than current methods that use prostate-specific antigen (PSA). If effective
EN2_(gene)
Protein-coding gene in humans
lethal condition is known as posterior amelia with pelvic and pulmonary hypoplasia syndrome (PAPPAS). Mutations in TBX4 associated with small patella syndrome
TBX4
Class of ribonucleic acid that is not translated into proteins
controls. Mutations within RNase MRP have been shown to cause cartilage–hair hypoplasia, a disease associated with an array of symptoms such as short stature
Non-coding_RNA
Transcription factor gene of the regulatory factor X family
syndrome, which is characterized by neonatal diabetes with pancreatic hypoplasia, duodenal and jejunal atresia, and gall bladder agenesis. GRCh38: Ensembl
RFX6
MADH4 Pontocerebellar hypoplasia type 1; 607596; VRK1 Pontocerebellar hypoplasia type 2A; 277470; TSEN54 Pontocerebellar hypoplasia type 2B; 612389; TSEN2
List_of_OMIM_disorder_codes
Protein-coding gene in the species Mus musculus
component of RNase MRP, which causes pleiotropic human disease cartilage–hair hypoplasia. Also, as patients with acute lymphoblastic leukemia often carry genetic
FAM221B
estrogen as a monthly contraceptive in nulliparous women with mild uterine hypoplasia". Am. J. Obstet. Gynecol. 112 (4): 575–6. doi:10.1016/0002-9378(72)90319-5
Pharmacodynamics_of_estradiol
InterPro Family
inhibited result in birth defects such as failure of the wall to close, hypoplasia of the musculature, and other defects. Following the formation of the
Protein_Wnt-6
Medical condition
oligohydramnios, to try to limit the associated lung underdevelopment, or pulmonary hypoplasia, that is seen at birth in these patients. The risks of fetal surgery are
Posterior_urethral_valve
Chemical compound
treatment of gynecological disorders. It is also used in the treatment of prostate cancer in men. Estradiol benzoate is used in veterinary medicine as well
Estradiol_benzoate
Erectile female sexual organ
congenital abnormalities of the clitoris may also include agenesis or hypoplasia. ... After the 13th to 14th weeks of gestation, androgen exposure produces
Clitoris
Medical condition
secretion from the anterior pituitary. The uterus and endometrium show hypoplasia and hypotrophy, respectively, and the vagina is atrophic. The oviduct
Estrogen insensitivity syndrome
Estrogen_insensitivity_syndrome
Branch of medicine
agenesis Mayer-Rokitansky-Küster-Hauser syndrome Vulvar abnormalities Labial hypoplasia Labial hypertrophy Source: Cryptorchidism Hypospadias Epispadias Source:
Reproductive_medicine
Human chromosome
thrombocytopenic purpura trisomy 9 tuberous sclerosis VLDLR-associated cerebellar hypoplasia G-banding ideograms of human chromosome 9 "Search results - 1[CHR] AND
Chromosome_9
Medical condition
karyotype) XX gonadal dysgenesis (46,XX karyotype) Leydig cell agenesis or hypoplasia, not otherwise specified (46,XY karyotype) Absent (vanishing) testes syndrome
Androgen insensitivity syndrome
Androgen_insensitivity_syndrome
Pain during sexual intercourse
remnants, tight hymenal ring, vaginal septa, thickened undilatable hymen, hypoplasia of the introitus, retroverted uterus or uterine prolapse can contribute
Dyspareunia
Mammalian protein found in humans
(January 2001). "Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8". The Journal of Clinical Endocrinology
PAX8
Atypical congenital variations of sex characteristics
"Mechanism of the Dual Activities of Human CYP17A1 and Binding to Anti-Prostate Cancer Drug Abiraterone Revealed by a Novel V366M Mutation Causing 17,20
Intersex
Protein-coding gene in the species Homo sapiens
inherited anonychia, is not mutated in a patient with congenital nail hypoplasia/aplasia with underlying skeletal defects". The British Journal of Dermatology
R-spondin_4
Protein-coding gene in the species Homo sapiens
result in craniofacial abnormalities such as cleft palate, mandibular hypoplasia, or tooth agenesis. In conclusion, FGF8 expression has effects on a person’s
Fibroblast_growth_factor_8
Medical condition
mutations that cause PAIS are also associated with prostate and breast cancers. Vaginal hypoplasia, a relatively frequent finding in CAIS and some forms
Partial androgen insensitivity syndrome
Partial_androgen_insensitivity_syndrome
Medical condition
Hypopituitarism Inborn errors of steroid metabolism Kallmann syndrome Leydig cell hypoplasia Sex hormones Pitteloud, Nelly; Hayes, Frances J.; Boepple, Paul A.; DeCruz
Gonadotropin-releasing hormone insensitivity
Gonadotropin-releasing_hormone_insensitivity
Electric current produced in living cells
upper lip, flattened philtrum, micrognathia, dental oligodontia, enamel hypoplasia, delayed dentition eruption, malocclusion, broad forehead, wide set eyes
Developmental_bioelectricity
Protein-coding gene in humans
playing a role in human prostate cancers. Mutations within PAX2 have been shown to result in optic nerve colobomas and renal hypoplasia. Alternative splicing
PAX2
treatable with phenobarbital and supportive antiepileptics. Cerebellar hypoplasia is an incomplete development of the cerebellum. The most common cause
List_of_dog_diseases
Mammalian protein found in humans
H, et al. (April 2003). "Dax-1 (dosage-sensitive sex reversal-adrenal hypoplasia congenita critical region on the X chromosome, gene 1) gene transcription
Catenin_beta-1
Application of fine-needle aspiration
male infertility. Recognized patterns include: normal spermatogenesis, hypoplasia or hypospermatogenesis, complete or early maturation arrest, Sertoli cell-only
FNA_mapping
Glycoprotein involved in neuronal migration
considered to be the cause of the rare form of lissencephaly with cerebellar hypoplasia classed as a microlissencephaly called Norman-Roberts syndrome. The mutations
Reelin
Language used to describe the human body
(change in cell or tissue phenotype) Hyperplasia (proliferation of cells) Hypoplasia (congenital below-average number of cells, especially when inadequate)
Medical_terminology
Protein
et al. (February 2004). "Expression of androgen receptor coregulators in prostate cancer". Clinical Cancer Research. 10 (3): 1032–40. doi:10.1158/1078-0432
Nuclear_receptor
Protein-coding gene in the species Homo sapiens
(December 1999). "Infertility in adult hypodactyly mice is associated with hypoplasia of distal reproductive structures". Biology of Reproduction. 61 (6): 1402–1408
HOXA13
Protein-coding gene in the species Homo sapiens
by a number of clinical features including mammary and apocrine gland hypoplasia, upper limb defects, malformations of areola, dental structures, heart
TBX3
Protein-coding gene
human BodyMap Project, but relatively abundant in adipose, colon, lung, prostate and skeletal muscle tissues. Human MAFF gene is induced by proinflammatory
MAFF_(gene)
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PROSTATE HYPOPLASIA
PROSTATE HYPOPLASIA
Surname or Lastname
English
English : variant of Prestwich, reflecting the old local pronunciation of the place name.
Boy/Male
Arabic, Muslim
One who Prostrates to the Merciful
Boy/Male
Indian
One who prostrates to the merciful (Allah)
Girl/Female
Indian
Prostrate in worship, Bowing
Boy/Male
Muslim
One who prostrates to the merciful (Allah)
Boy/Male
Arabic, Muslim
One who Prostrates to the Merciful Allah
Girl/Female
Muslim
Prostrate in worship, Bowing
Girl/Female
Arabic, Australian, Muslim, Pashtun
Prostrate in Worship
PROSTATE HYPOPLASIA
PROSTATE HYPOPLASIA
PROSTATE HYPOPLASIA
PROSTATE HYPOPLASIA
PROSTATE HYPOPLASIA
PROSTATE HYPOPLASIA
PROSTATE HYPOPLASIA
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