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Developmental anomalies
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Part 1 book "Textbook of veterinary pathology - Quick review and self assessment" includes content: Introduction, etiology, genetic disorders, developmental anomalies and monsters, disturbances in growth, disturbances in circulation, disturbances in cell metabolism, necrosis, gangrene and post mortem changes, disturbances in calcification and pigment metabolism, inflammation and healing, concretions, immunity and immunopathology, pathology of cutaneous system, pathology of musculoskeletal systemm,... and other contents.
311p
muasambanhan10
06-04-2024
3
1
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Smith-Magenis syndrome (SMS) is a developmental disability/multiple congenital anomaly disorder resulting from haploinsufficiency of RAI1. It is characterized by distinctive facial features, brachydactyly, sleep disturbances, and stereotypic behaviors.
15p
vioraclene
31-03-2024
4
2
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Say–Barber–Biesecker–Young–Simpson (SBBYS) (OMIM #603736, Ohdo syndrome variant) is a rare type of severe blepharophimosis intellectual disability syndrome, which is generally characterized by a global developmental delay, distinctive facial features, and intellectual disability with multiple congenital anomalies, including skeletal involvement, missing, or underdeveloped kneecaps, and genital anomalies, in affected males.
7p
vitiki
30-01-2024
4
2
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Agenesis of the right hepatic lobe is a rare congenital anomaly. Developmental anomalies of the right lobe of the liver were first reported in 1870 by Heller. Anatomical variations of the liver are common, occur during the normal development of the organ, and correspond to variations in the distribution of liver territories.
8p
vitiki
30-01-2024
5
2
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Part 1 book "Textbook of veterinary pathology" includes content: Introduction; etiology; genetic disorders, developmental anomalies and monsters; disturbances in growth; disturbances in circulation; disturbances in cell metabolism; necrosis; gangrene and post mortem changes; disturbances in calcification and pigment metabolism; concretions, immunity and immunopathology, pathology of cutaneous system, pathology of musculoskeletal system, pathology of cardiovascular system, pathology respiratory system,... and other contents.
353p
muasambanhan05
22-01-2024
4
2
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Congenital heart diseases are occasionally encountered in the bovine species. Ventricular septal defects (VSD) and atrial septal defects (ASD) are reported to be the most common; However, a vast collection have been reported.
7p
vigandhi
23-02-2022
12
1
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Microdeletion of chromosome 22q11 is associated with significant developmental anomalies, including disruption of the cardiac outflow tract, thymic/parathyroid aplasia and cleft palate. Amongst the genes within this region, TBX1 is a major candidate for many of these developmental defects.
20p
vibeauty
23-10-2021
4
0
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Copy number variants (CNVs) have been shown to increase risk for physical anomalies, developmental, psychiatric and medical disorders. Some of them have been associated with changes in weight, height, and other physical traits.
9p
vitzuyu2711
29-09-2021
8
1
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Loss of proprotein convertase subtilisin/kexin type 5 (Pcsk5) results in multiple developmental anomalies including cardiac malformations, caudal regression, pre-sacral mass, renal agenesis, anteroposterior patterning defects, and tracheo-oesophageal and anorectal malformations, and is a model for VACTERL/caudal regression/Currarino syndromes (VACTERL association - Vertebral anomalies, Anal atresia, Cardiac defects, Tracheoesophageal fistula and/or Esophageal atresia, Renal & Radial anomalies and Limb defects).
10p
viwyoming2711
16-12-2020
11
1
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This syndrome is defined by an extremely wide spectrum of characteristics; however, developmental delay and intellectual disability of various degree are present in all patients and about the 90% of patients have a severe intellectual disability. Dental agenesis or other dental anomalies have not been described in previous reports.
7p
viorochimaru2711
29-05-2020
12
1
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part 1 book “textbook of oral medicine” has contents: development and eruption of teeth, development and anatomy of craniofacial region, infection control in dental office, neoplasm, investigation in dentistry, case history, teeth anomalies, developmental defect of craniofacial structure, keratotic and nonkeratotic lesions,… and other contents.
531p
tieu_vu13
06-08-2018
33
2
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(bq) part 1 book "oral medicine and pathology at a glance" presentation of content: examination of extraoral tissues, anatomical variants and developmental anomalies, blisters, pigmented lesions, red and purple lesions, ethnic pigmentation and tattoos,... and other contents.
61p
thangnamvoiva23
06-10-2016
27
5
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(BQ) Part 1 of the document Color atlas of oral diseases presents the following contents: Normal anatomic variants, developmental anomalies, genetic diseases, mechanical injuries, oral lesions due to chemical agents, oral lesions due to smoking and heat, oral lesions due to drugs,..
199p
thangnamvoiva5
14-07-2016
51
5
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(BQ) Part 1 of the document Diagnostic imaging obstetrics presents the following contents: First trimester, brain (abdominal wall and gastrointestinal tract, midline developmental anomalies, cranial defects,...), spine, face and neck, chest, abdominal wall and gastrointestinal tract.
791p
thangnamvoiva4
01-07-2016
49
2
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(BQ) Part 1 of the document Diagnostic imaging of infants and children presents the following contents: Neonatal lung disease, pulmonary infection, the mediastinum, congenital heart disease, anomalies of the great vessels, the breast, developmental abnormalities of the lungs and diaphragm,...
501p
thangnamvoiva4
01-07-2016
57
8
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HIC1(hypermethylated in cancer) is a tumour suppressor gene located in 17p13.3, a region frequently hypermethylated or deleted in many types of prevalent human tumour.HIC1is also a candidate for a contiguous-gene syndrome, the Miller–Dieker syndrome, a severe form of lissencephaly accompanied by developmental anomalies.
12p
inspiron33
25-03-2013
33
2
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