Cytogenetic and clinical study on 100 cases of primary amenorrhoea

  • 78 Pages
  • 3.31 MB
  • English

Departments of Obstetrics and Gynecology, University Central Hospital , Helsinki
Amenorrhea -- Case studies., Amenorrhea -- Statistics., Cytogene
StatementHanna Kallio
GenreCase studies., Statistics.
ContributionsKallio, Hanna.
LC ClassificationsRG"171"K34
The Physical Object
Pagination78 p. :
ID Numbers
Open LibraryOL20021614M

To study the prevalence of chromosomal abnormalities and the different options available for clinical management of women in Mexico with primary amenorrhoea, a cross-sectional study. Cytogenetic studies in amenorrhea. study, women with primary amenorrhoea were evaluated.

Chromosomal analysis of all the cases was.

Details Cytogenetic and clinical study on 100 cases of primary amenorrhoea FB2

A comprehensive evaluation is not necessary for most women under the age of 16 years, but is for women over 16 years, especially if there is a family history of primary amenorrhea, ambiguous genitalia, or evidence of an endocrinopathy that may affect menstrual function.

Clinical Obstetrics and Gynecology, 16,3. Jones, K. () Feminization, virilization and precocious sexual development that results from neoplastic processes. A nnals of the New York Academ y of Sc iences,Kallio.

() Cytogenetic and Clinical Study on Cases ofPrimary Amenorrhoea. Helsinki: Vammalan Kirjapaino Oy. Cited by: 1. Triple X syndrome (47,XXX) is not extremely rare, although one might think so, as the majority of cases go undiagnosed.

1 The incidence has been established to 1/ females, since the earliest case series have been published and confirmed by others. 2 Triple X syndrome is a sex chromosomal abnormality (SCA).Cited by: The aim of the study was to estimate prevalence, incidence and diagnostic delay in 46,XY females in an unselected population in a nationwide study.

Design: A retrospective cohort study. Patients and methods: From the Danish Cytogenetic Registry data of all cases registered as females and diagnosed wXY or a related male karyotype in Author: Agnethe Berglund, Kirstine Stochholm, Jens Fedder, Gravholt Claus Hojbjerg.

This banner text can have markup. web; books; video; audio; software; images; Toggle navigation. Clinical profile of patients of head and neck cancers- a prospective study of cases. A clinical study to compare between unstimulated and stimulated whole salivary flow rate before and after complete denture placement in diabetic and non diabetic patients Primary amenorrhoea: our experience from a tertiary care centre.

Clinical characteristics. Blephariphimosis, ptosis, and epicanthus inversus syndrome (BPES) is a complex eyelid malformation invariably characterized by four major features: blepharophimosis, ptosis, epicanthus inversus, and type I includes the four major features and premature ovarian insufficiency (POI); BPES type II includes only.

The word “lethal” is used by geneticists in a relative sense. They regard a genetic defect as lethal if it prevents the possessor from reproducing itself through premature death. If the defective Cited by: 4. The Global Library of Women’s Medicine is dedicated to the memory of Abigail Bloomer, just one of far too many lovely women who die too young from diseases or conditions that are gender specific.

We feel that we owe it to them all to try harder and care better every day.

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expert chapters. Critical Current Issues. Safer Motherhood. Cytogenetic, biochemical, biophysical and interventional diagnostic procedures are necessary only to corroborate the clinical diagnosis and in few cases where the clinical diagnosis remains disputed.

Hence, the indications of special investigations should be oriented on the basis of clinical approach. The risk of developing breast cancer is fold and 40–80% of cases occur before the age of 70 years The prognosis in these women is the same as for sporadic cases. Early age of onset of breast cancer.

Male breast cancer (6% in males with BRCA 2 gene mutation) Coexistence of ovarian and breast cancer in the same family. Raine - Cases in Paediatrics () код для вставки ).

Cytogenetic analysis in products of conception (poc) cases: our experience of past 19 years. ISAR1 st MarchMumbai. Arundhati Athalye, Dhanashree Warang, Prashant Padyal, Smita Gavas, Firuza ance of preimplantation genetic screening (PGS) in cases with preimplantation genetic diagnosis (PGD) for monogenic disorders.

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Who was being treated with hormone replacement therapy (HRT) for primary amenorrhoea. In most cases, however, a history of secondary amenorrhoea excludes congenital abnormalities.

A family history of fertility problems, autoimmune disorders or premature menopause may also give clues to the aetiology/5. The diagnosis is made by clinical examination with particular attention to posture, pattern of tone in the limbs and trunk, hand function and gait. An MRI may show the cause of CP but it will not diagnose CP.

There are three main clinical subtypes: spastic (90%), dyskinetic (6%) and ataxic (4%). A mixed pattern may occur. Dear AGOI colleagues, Warm Greetings from AGOI. The scientific committee of ASGO has extended the deadline of abstract submission until Jin order to make more exciting meeting with sharing the latest researches and studies of doctors from India.

You can Submit abstract and participate in ASGO meeting. Disclaimer. Oxford University Press makes no representation, express or implied, that the drug dosages in this book are correct.

Readers must therefore always check the product information and clinical procedures with the most up to date published product information and data sheets provided by the manufacturers and the most recent codes of conduct and safety regulations. Full text of "Short Cases In Clinical Medicine 5th Edition By ABM Abdullah" See other formats.

DSD are typically categorized in disorders of sex determination and disorders of sex differentiation (see Fig. ).In the former, the development of the gonads is disrupted, and leads to either gonadal dysgenesis, or the development of by:   Infertility is defined as the inability to become pregnant after 12 months of regular, unprotected intercourse.

In a survey from toCited by:   Left gonad had homogenous echotexture. Pelvic ultrasound examination showed no evidence of a uterus or ovaries. The testosterone levels were measured both were in the normal range (3- 10ng/ml).

Cytogenetic analysis performed on peripheral blood lymphocytes revealed a 45,XX/46,XY karyotype. Case Study No 1 OTS. Gonadectomy with biopsy   2. Cytogenetic studies in haematological malignancies.

(From tofunded by Dept. of Science & Technology, Kerala State). Cytogenetic studies in children with congenital abnormalities. (From tofunded by SAT Hospital Endowment Fund). Search for biological markers in premalignant and malignant lesions of oral cavity. Unfortunately, this book can't be printed from the OpenBook.

If you need to print pages from this book, we recommend downloading it as a PDF. Visit to get more information about this book, to buy it in print, or to download it as a free PDF. Cancer is associated with a wide range of hereditary disorders. Recognizing these disorders in cancer patients may be of great importance for the medical management of both patients and their relatives.

Conversely, recognizing the fact that cancer may develop as a complication of a particular hereditary disorder which has already been diagnosed may be Cited by: 4.

The aim of this book is to provide a straightforward summary of the knowledge required for examinations in specialist Obstetrics and Gynaecology. Part Two of the examination for Membership of the Royal College of Obstetricians and Gynaecologists would be a good example.

(primary) in more than 45% of cases. In another 30% cases titres may be low but positive. • Weakly positive and low titres may also be found in patients with. The potential to have somatic intersex variations exists (however, briefly) in all humans’ prenatal development in the first few weeks—for a portion of humans, a level of ambiguity in their sex traits continues on after this point (Ainsworth, ).Intersex variations are atypical sex characteristics (Organisation Intersex International [OII] Australia, b); these Cited by: 4.

Eighty to 90% of cases of primary hyperparathyroidism are due to solitary parathyroid adenoma, with only 1% due to parathyroid carcinoma. Giant parathyroid adenoma is. In this study, major clinical manifestations of DSD cases were evaluated separately.

In Turner syndrome most common presentation was primary amenorrhoea (% in classic and % in mosaic Turner syndrome) followed by short stature (% in classic Turner syndrome).Hanford radiation study III: a cohort study of the cancer risks from radiation to workers at Hanford ( deaths) by the method of regression models in life-tables.

Brit J Ind Med Knox, E.G. year-old girl with primary amenorrhoea, height cm, weight 51 kg, well developed breast, no pubic or axillary hair and no hirsutism. Most probable diagnosis is Complete androgen insensitivity syndrome.

year-old woman with secondary amenorrhoea for 3 years along with galactorrhoea. Most likely cause of her symptoms would be Prolactinoma.