Results 21 to 30 of about 2,355 (68)

A head start: The relationship of placental factors to craniofacial and brain development

Developmental Dynamics, EarlyView.
Abstract In recent years, the importance of placental function for fetal neurodevelopment has become increasingly studied. This field, known as neuroplacentology, has greatly expanded possible etiologies of neurodevelopmental disorders by exploring the influence of placental function on brain development.
Annemarie Jenna Carver, Martine Dunnwald, Hanna Elizabeth Stevens   +2 more
wiley   +1 more source

Neuropathic-like pain in fibrous dysplasia/McCune-Albright syndrome [PDF]

, 2022
Context: Pain is a major symptom in adults with fibrous dysplasia/McCune-Albright syndrome (FD/MAS) and response to current treatments, including bisphosphonates and standard analgesics (nonsteroidal anti-inflammatory drugs and opiates) is unpredictable.
Boyce, Alison M, Heegaard, Anne-Marie, Javaid, Muhammad, Pinedo-Villanueva, Rafael, Soni, Anushka, Spencer, Tiahna L, Watts, Laura   +6 more
core   +2 more sources

Occurrence of testicular microlithiasis in androgen insensitive hypogonadal mice [PDF]

, 2009
<b>Background</b>: Testicular microliths are calcifications found within the seminiferous tubules. In humans, testicular microlithiasis (TM) has an unknown etiology but may be significantly associated with testicular germ cell tumors ...
AC Peterson, Ana Monteiro, BM Cattanach, C Lecureuil, CE Hoei-Hansen, DL Lam, Guido Verhoeven, HH Rashid, J Coffey, J Lang, K De Gendt, K Thomas, Karl De Gendt, L Murphy, LA Korde, M Nistal, M Nistal, M Vegni-Talluri, M Wasniewska, Margaret H Abel, NJ van Casteren, Peter J O'Shaughnessy, R Drut, RA Rey, S Zastrow   +24 more
core   +2 more sources

Secondary amenorrhea in a case of gonadotropin independent precocious puberty: McCune-Albright syndrome [PDF]

, 2021
Precocious puberty may be gonadotropin dependent or gonadotropin independent and due to a myriad of causes including syndromic association. McCune-Albright syndrome (MAS) is a rare disorder, characterized by the triad of precocious puberty, polyostotic ...
Jayaraman, Sangumani, Natarajan, Sundari, Nazirudeen, Roshan, Subbiah, Sridhar, Vasanthiy, Vasanthiy   +4 more
core   +2 more sources

Management of infertility in a patient presenting with ovarian dysfunction and McCune-Albright syndrome [PDF]

, 2004
Persistent autonomous ovarian dysfunction in McCune-Albright syndrome (MAS) patients is associated with the development of multiple dominant follicles, premature luteinization, cyst formation, and anovulatory infertility.
Fauser, B.C.J.M. (Bart), Laven, J.S.E. (Joop), Lumbroso, S., Sultan, C.   +3 more
core   +2 more sources

Leptomeningeal Seeding of Pituitary Adenoma in a Young Lady With Neglected Gigantism: An Extremely Rare Case Report

Clinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT Pituitary neuroendocrine tumors can sometimes present with leptomeningeal seeding at their initial diagnosis, emphasizing the need for thorough evaluation in cases of leptomeningeal involvement. Additionally, it is crucial for general physicians to inquire about a patient's menstrual status, particularly in low socioeconomic conditions, as ...
Sadegh Bagherzadeh, Milad Shafizadeh, Seyed Mohammad Tavangar, Alireza Khoshnevisan   +3 more
wiley   +1 more source

Evolução da displasia fibrosa óssea na síndrome de McCune Albright [PDF]

, 1999
McCune Albright syndrome is a rare disorder characterized by polyostotic fibrous dysplasia, café-au-lait spots and some endocrine hyperfunction, mostly precocious puberty.
Dias-da-Silva, Magnus Régios [UNIFESP], Farhat, Helena L. [UNIFESP], Lazaretti-Castro, Marise [UNIFESP], Verreschi, Ieda Therezinha do Nascimento [UNIFESP]   +3 more
core   +2 more sources

A Rare Case of ACTH‐Secreting Pituitary Adenoma in a Pediatric Patient. Diagnosis and Management: Case Report and Literature Review

Clinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT Due to its rare incidence, pituitary adenoma requires high vigilance and suspicion. Therefore, physicians should consider this differential diagnosis and perform the necessary workup, such as an overnight or standard dexamethasone suppression test and brain magnetic resonance imaging (MRI), to rule it out if sudden hormonal changes without any
Shadi Niliyeh, Fatemeh Sayarifard, Ali Moradi, Aria Setoodeh, Pouya Ebrahimi   +4 more
wiley   +1 more source

Polyostotic Fibrous Dysplasia With and Without McCune-Albright Syndrome-Clinical Features in a Nordic Pediatric Cohort [PDF]

, 2018
Objective: Fibrous dysplasia (FD) presents as skeletal lesions in which normal bone is replaced by abnormal fibrous tissue due to mosaic GNAS mutation.
Bjornsdottir, Sigridur, Horemuzova, Eva, Mäkitie, Outi, Utriainen, Pauliina, Valta, Helena   +4 more
core   +1 more source

Post‐COVID‐19 Exacerbation of a Stable Fibrous Dysplasia: A Case Report

Clinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT Fibrous dysplasia (FD) is a rare, benign fibro‐osseous lesion characterized by replacement of normal bone with extensive fibrous stroma due to abnormalities in osteoblast differentiation. After puberty and during adulthood, FD lesions usually become quiescent. However, some cases show signs of regrowth and reactivation.
Mohammed Taib Fatih, Mohammed Abdalla Mahmood, Mohammed Khalid Mahmood, Amanj Ismael Tahir, Handren Ameer Kurda, Mohammed Aso Abdulghafor, Balen Hamid Qadir, Zana Fuad Noori   +7 more
wiley   +1 more source