Results 41 to 50 of about 1,463 (166)

Isolated Hypoglossal Nerve Palsy as an Initial Presentation of Metastatic Breast Cancer in Pregnancy: A Case Report

Progress in Neurology and Psychiatry, Volume 30, Issue 2, May 2026.
ABSTRACT Isolated hypoglossal nerve palsy is rare, with neoplastic causes representing the most common etiology. We present an unusual case of metastatic breast cancer presenting with isolated hypoglossal nerve palsy during pregnancy. A 36‐year‐old primigravida at 17 weeks of gestation was admitted with progressive immobility, worsening back pain, and ...
Nalini Kurri, Muhammad Ibrahim Memon, Shaguna Chandran, Adnan Agha   +3 more
wiley   +1 more source

Parry Romberg syndrome: A rare case report

Journal of Indian Academy of Oral Medicine and Radiology, 2014
The Parry Romberg syndrome (PRS) is a rare neurocutaneous disorder characterized by progressive facial hemiatrophy. Parry Romberg syndrome is characterized by a slow progressive atrophy that appears in the early stages of life, primarily affecting the ...
Raj Kumar Badam, Balaji Gandhi Babu Dara, Srinivas Rao Pallerla, Mamatha Boringi   +3 more
doaj   +1 more source

Facial Hemiatrophy in a Monomania [PDF]

The Journal of Nervous and Mental Disease, 1883
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openaire   +1 more source

Assessing Optic Nerve Involvement in Multiple Sclerosis Using Optical Coherence Tomography and Magnetic Resonance Imaging

European Journal of Neurology, Volume 33, Issue 4, April 2026.
The IED cutoff (GCIPL ≥ 4 μm or pRNFL ≥ 6 μm) showed 83% sensitivity and 55% specificity for detecting prior optic neuritis, and 67% sensitivity with 83% specificity for identifying asymptomatic optic nerve lesions in patients without prior history of optic neuritis.
Gualco Alessandro, Boffa Giacomo, Razzetta Chiara, Lapucci Caterina, Cipriano Emilio, Nasone Lorenza, Sirito Tommaso, Al Qudsi Sabrina, Garbarino Sara, Saitta Laura, Campi Cristina, Iester Michele, Cellerino Maria, Inglese Matilde   +13 more
wiley   +1 more source

Dyke–Davidoff–Masson syndrome with crossed cerebellar atrophy

South African Journal of Radiology, 2017
Dyke–Davidoff–Masson syndrome is a rare condition with classical, clinical and radiological changes – mental retardation, hemiparesis, facial asymmetry, seizures and cerebral hemiatrophy with calvarial changes.
Sanjay M. Khaladkar, Shishir Chauhan, Abhijit M. Patil, Siddappa G. Gandage, Surbhi Chauhan Kalra   +4 more
doaj   +1 more source

A case of partial anomalous systemic venous drainage and perioperative detection of cerebral arteriovenous malformations

Annals of Pediatric Cardiology, 2021
We report a case of 8-year-old boy with unexplained desaturation and clubbing. Echocardiography showed anomalous drainage of right superior vena cava into left atrium. He did not have any neurological symptoms preoperatively.
Nilanjan Dutta, Debasis Das, Raghu Maruti Govindappa, Patralekha Das, Rangan Koley, Manish Kumar Sharma, Amitabha Chattopadhyay, Sanjiban Ghosh   +7 more
doaj   +1 more source

A review of pediatric cerebral hemiatrophy: a series of cases

MGM Journal of Medical Sciences
Cerebral hemiatrophy represents a spectrum of neurological disorders marked by unilateral cerebral atrophy, often resulting in significant neurological and functional impairments.
Sumedha Varshney, Rahul Ranjan, Nirmal Pandey, Namrata, Ashok Yadav, Ramesh Chandra Rajput   +5 more
doaj   +1 more source

Adult Presentation of Dyke-Davidoff-Masson Syndrome: A Case Report

Case Reports in Neurology, 2016
Dyke-Davidoff-Masson syndrome (DDMS) is a rare disease which is clinically characterized by hemiparesis, seizures, facial asymmetry, and mental retardation.
Ujjawal Roy, Ajay Panwar, Adreesh Mukherjee, Debsadhan Biswas   +3 more
doaj   +1 more source

Facial hemihypertrophy and facial hemiatrophy: Report of 2 cases

Journal of Indian Academy of Oral Medicine and Radiology, 2008
Facial hemihypertrophy and facial hemiatrophy are rare developmental anomalies. These conditions are characterized by an asymmetric growth of one or more parts of the tissues on one side of the face. The facial asymmetry may be total or partial.
Atul Indurkar, Shirish Degwekar, Shailesh Gondivkar   +2 more
doaj   +1 more source

Epidermal Nevi and Epidermal Naevus Syndromes

JEADV Clinical Practice, Volume 4, Issue 3, Page 669-680, August 2025.
ABSTRACT Epidermal nevi (EN) arise from postzygotic variants in ectoderm‐derived cell lines, such as keratinocytes and cells forming adnexa. EN may be present alone without any associated abnormality or be part of a syndrome. In this review, we will discuss about the clinical and genetics of the main types of EN and related syndromes.
Gianluca Tadini, Beatrice Carcano, Michela Brena   +2 more
wiley   +1 more source