User:Mariamhanna21/sandbox
| Mariamhanna21/sandbox | |
|---|---|
| Other names | Spontaneous periodic hypothermia |
| Specialty | Neurology |
Abstract
Shapiro syndrome is an extremely rare disorder consisting of paroxysmal hypothermia (due to hypothalamic dysfunction of thermoregulation), hyperhydrosis (sweating), and agenesis of the corpus callosum with onset typically on adulthood. The disease affects about 50 people worldwide. The duration and frequency of the episodes vary from person to person, with some episodes lasting hours to weeks and occurring from hours to years. Very little is known about the disease due to the small number of people affected.[1] While Shapiro Syndrome typically affects adults, it can be prevalent in children as well. In this article, symptoms of Shapiro syndrome, the cause, pathophysiology, and diagnostics will be discussed. Alongside, treatment and management of the disease, prognosis, epidemiology, and research direction.
Signs and Symptoms:
Common symptoms of Shapiro syndrome are hypothermia and Hyperhidrosis associated with agensis of the Corpus callosum.[2] Individuals will present with a core body temperature that is below 35 degrees Celsius. Recurrent hypothermia can occur spontaneously at any time. Individuals will also present with profuse sweating, mainly in the upper body and face. Sweating episodes can last 1-2 hours. Other symptoms can include nausea, vomiting, chills, altered consciousness, and a feeling of weakness.
Cause:
Some possible causes of Shapiro syndrome include hypothalamic dysfunction, neurotransmitter abnormalities, genetic variation, and endogenous high melatonin. However, the exact cause of Shapiro syndrome is unknown. Hypothalamus is a structure deep within the brain that connects the endocrine and nervous system together. The hypothalamus keeps the body in homeostasis. Dysfunction in the hypothalamus can lead to the body temperature fluctuations. Neurotransmitter are the chemical messengers that carry signals between nerve cells, muscles, and glands in the body. Previous studies have confirmed that Dopamine and Serotonin are associated with the development of Shapiro syndrome. It has been shown that specific serotonin dysfunction in the extrapyramidal shivering mechanism in the anterior hypothalamus is central to the pathogenesis of paroxysmal spontaneous hypothermia with hyperhidrosis.[2] Melatonin is a hormone that is the secreted from the pineal gland. Melatonin is the regulator of the sleep-wake cycle and plays a role in thermoregulation. In recent studies, it has been shown that hypermelatonemia could be associated with the development of Shapiro Syndrome. However, only one case out of the 50-60 reported had hypermelatonemia.[2] Agenesis of the corpus callosum (ACC) is a rare, congenital brain defect that occurs when the corpus callosum does not develop normally. ACC involves the partial or complete loss of the main connectivity pathway connecting the two brain hemispheres and may be isolated. [3] In majority of cases, ACC is caused by genetic factors. Genetic factors can include single gene mutations, multiple gene changes, and chromosomal aberrations.[4] There is no definitive prevention for Shapiro syndrome.
Mechanism of Disease:
Shapiro syndrome develops when there is hypothalamus dysfunction. The hypothalamus is the body's primary thermostat. A decrease in the "set point" temperature leads to the development of Shapiro syndrome. Agenesis of the corpus callosum can lead to the development of Shapiro syndrome.The corpus callosum ensures that the two brain hemispheres communicate with each other. When the corpus callosum is missing or not formed properly, it can lead to many dysfunctions throughout the body including hypothermia and hyperhidrosis. Agenesis of the corpus callosum has been found in 40% of Shapiro syndrome cases reported. [5] It is theorized that Shapiro syndrome develops based on genetic factors. However, the true mechanism of development of the disease and what causes it remains unknown.
Diagnosis:
If an individual is suspected of having Shapiro syndrome, a neurologist would be able to confirm the diagnosis. If an individual is experiencing spontaneous episodes of hypothermia along with hyperhidrosis, a neurologist could suspect Shapiro syndrome. In order to confirm the diagnosis of Shapiro syndrome, an MRI of the brain would be conducted. If the MRI confirms agenesis of the corpus callosum, then the individual could be diagnosed with Shapiro Syndrome. Getting diagnosed with Shapiro syndrome is very difficult because there are no reliable imaging or laboratory test to diagnose Shapiro Syndrome.[2] Since Shapiro syndrome is quite rare, individuals are often misdiagnosed with meningitis or Autoimmune encephalitis.
Treatment or Management:
There are currently no treatment options for Shapiro syndrome. However, there are medications that can help with management for some of the symptoms. One of the major symptoms of Shapiro syndrome is the hypothermia. Clonidine, an alpha 2-adrenoreceptor agonist, was associated with a return to normal central temperature regulation.[6] Clonidine is the most commonly used medication for hypothalamic regulation. However, medications that can mimic neurotransmitters that affect the hypothalamus can be used to help with regulating hypothalamic dysfunction. Medications such as gabapentin, venlafaxine, chlorpromazine, and levodopa-carbidopa may be used to mimic neurotransmitter activity.
Prognosis:
Although Shapiro syndrome is common in young adults, Shapiro syndrome cases have been reported in individuals from 8 months to 80 years old. Studies have shown that Shapiro syndrome development might be associated with genetic factors, however data is limited on the impact of the genetics on Shapiro syndrome. Hypothermia episodes in individuals with Shapiro syndrome can be expected to reoccur throughout their lifetimes. However, medications that regulate the hypothalamus, such as clonidine, can help with alleviating the hypothermic episodes.[6] Prognosis data is limited for Shapiro syndrome since less than 60 cases have been reported worldwide.
Epidemiology:
Due to Shapiro syndrome being extremely rare and underdiagnosis, its prevalence is not well defined. Through studies, it has been shown that genetic background can have an influence on the development of Shapiro syndrome. Limited research has explored how environmental influence might interact with genetic predispositions to trigger or exacerbate symptoms. The disease can manifest in any age, gender, and ethnicity. However, most cases that were reported were present in adulthood.
Research Directions:
Their have been studies conducted to determine what leads to the development of Shapiro syndrome. Some studies have linked the development of the disorder to hypothalamic dysfunction, neurotransmitter abornmalities, and agensis of the corpus callosum.[2] In 2022, a case study reported that hypoglycemia can be a potential manifestation of Shapiro syndrome.[7] However, this was only found in one the patients worldwide diagnosed with Shapiro syndrome. There is no current drug development for Shapiro syndrome, but some medications have been able to help with allievating symptoms. There are no confirmed current/upcoming clinical trials for Shapiro syndrome.
References
[edit]- ^ Shapiro Syndrome, Genetic and Rare Diseases Information Center (GARD), National Institutes of Health
- ^ a b c d e Ren, Linan; Gang, Xiaokun; Yang, Shuo; Sun, Meixin; Wang, Guixia (29 July 2022). "A new perspective of hypothalamic disease: Shapiro's syndrome". Frontiers in Neurology. 13. doi:10.3389/fneur.2022.911332. ISSN 1664-2295. PMC 9372501. PMID 35968294.
{{cite journal}}: CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link) - ^ Santo, S.; D'Antonio, F.; Homfray, T.; Rich, P.; Pilu, G.; Bhide, A.; Thilaganathan, B.; Papageorghiou, A. T. (2012-11). "Counseling in fetal medicine: agenesis of the corpus callosum". Ultrasound in Obstetrics & Gynecology. 40 (5): 513–521. doi:10.1002/uog.12315. ISSN 0960-7692.
{{cite journal}}: Check date values in:|date=(help) - ^ Palmer, Elizabeth Emma; Mowat, David (2014-06). "Agenesis of the corpus callosum: A clinical approach to diagnosis". American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 166 (2): 184–197. doi:10.1002/ajmg.c.31405. ISSN 1552-4868.
{{cite journal}}: Check date values in:|date=(help) - ^ Topcu, Yasemin; Bayram, Erhan; Karaoglu, Pakize; Yis, Uluc; Kurul, Semra Hiz (2013-12). "The combination of thermal dysregulation and agenesis of corpus callosum: Shapiro's or/and reverse Shapiro's syndrome". Annals of Indian Academy of Neurology. 16 (4): 716. doi:10.4103/0972-2327.120451. ISSN 0972-2327. PMC 3841640. PMID 24339619.
{{cite journal}}: Check date values in:|date=(help)CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link) - ^ a b Walker, B. R.; Anderson, J. A.; Edwards, C. R. (1992-03). "Clonidine therapy for Shapiro's syndrome". The Quarterly Journal of Medicine. 82 (299): 235–245. ISSN 0033-5622. PMID 1631258.
{{cite journal}}: Check date values in:|date=(help) - ^ Lewis, Connor; Freeman, Natasha; Gupta, Neil (13 March 2022). "Hypoglycemia as a Manifestation of Shapiro Syndrome". Cureus. doi:10.7759/cureus.23120. ISSN 2168-8184. PMC 9004329. PMID 35425687.
{{cite journal}}: CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link)
Further reading
[edit]- "Shapiro syndrome" Shenoy C. QJM. 2008 Jan;101(1):61-2. PMID 18203725
- "Shapiro syndrome with hypothalamic hypothyroidism" Arkader R, Takeuchi CA. Arq Neuropsiquiatr. 2008 Jun;66(2B):418-9. PMID 18641886
- "Subtotal corpus callosum agenesis with recurrent hyperhidrosis-hypothermia (Shapiro syndrome)" Tambasco N, Corea F, Bocola V. Neurology. 2005 Jul 12;65(1):124. PMID 16009897
External links
[edit]Category:Neurological disorders Category:Rare syndromes
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