Primary amenorrhoea caused by congenital absence of the uterus

2006 ◽  
Vol 275 (3) ◽  
pp. 199-201 ◽  
Author(s):  
E. J. Harland ◽  
M. Damodaram ◽  
L. Musaib-Ali ◽  
Wai Yoong
2016 ◽  
Vol 2 (2) ◽  
pp. 145-147
Author(s):  
Siva S ◽  
Divya Gopineni ◽  
Shafi P ◽  
Chandra Sekhar

Females with pituitary dwarfism and a multiple deficiency of pituitary hormones show ovarian dysfunction due to hypogonadotropism. Primary amenorrhea can be diagnosed if a patient has normal secondary sexual characteristics but no menarche by 16 years of age. A 16 year-old female patient admitted in general medicine department with chief complaints of shortness of breath on exertion since 15 days, swelling of both legs since 10 days, loss of weight since 5 months, loss of appetite since 3 months, history of pain during swallowing. Pelvis scan examination reveals that uterus measures 3.2×0.5×0.5cm; uterus is hypo plastic, ovaries not visualized. Patient parents reveled that from patient birth to 11years of age her growth and other developments were normal, after that her growth is stopped and no changes were observed in development since 5 years. Patient has hypothyroidism so pituitary gland make an important role to maintain hormone levels, pituitary gland produces thyroid stimulating hormone (TSH) which stimulates thyroid gland to produce thyroid hormones. Primary Amenorrhea, short stature and poorly developed secondary sexual characters which could have been contributed and should be subjected for karyotyping. This type of Pituitary Dwarfism is very difficult to manage.


2017 ◽  
Author(s):  
Elizabeth Burt ◽  
Antoinette Pimblett ◽  
Vikram Talaulikar ◽  
Ephia Yasmin ◽  
Dimitri Mavrelos ◽  
...  

2021 ◽  
Author(s):  
Shinya Inoue ◽  
Atsuo Mori ◽  
Yasunori Iida ◽  
Hidetoshi Oka

1993 ◽  
Vol 18 (3) ◽  
pp. 312-315 ◽  
Author(s):  
J. NAKAMURA ◽  
E. KUBO

A case of bilateral insertion of flexor pollicis longus to the proximal as well as the distal phalanges is reported. Initially, this case was diagnosed as congenital absence of the flexor pollicis longus, but surgery revealed an intact tendon, with the abnormality only present in the site of insertion. A survey of the literature on congenital abnormalities of flexor pollicis longus failed to reveal any reports of similar abnormalities.


1957 ◽  
Vol 74 (2) ◽  
pp. 397-404 ◽  
Author(s):  
John D. Thompson ◽  
Lawrence R. Wharton ◽  
Richard W. Te Linde
Keyword(s):  

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