Exploring the Connection Between Spinal and Renal Anomalies
I am a 29-year-old Caucasian woman with a medical history that includes hypermobile Ehlers-Danlos syndrome, cervical spondylosis, attention deficit hyperactivity disorder (ADHD), and an atrial septal defect (ASD). In short, I have two spinal vertebrae that exhibit incomplete segmentation, along with a duplex kidney. I recently stumbled upon information suggesting a correlation between spinal and renal malformations, which piqued my curiosity, prompting me to seek further details. After undergoing an MRI due to my cervical spondylosis, the results showed that my C6 and C7 vertebrae demonstrate “incomplete developmental segmentation.” So far, this has not resulted in any noticeable complications. However, I found this finding intriguing and decided to research it further. I discovered that the association between spinal deformities and kidney abnormalities is prevalent, yet the sources I consulted didn’t elaborate on the specifics of this connection. Since I also have a duplex kidney condition, I would appreciate more insight into this link, but my search yielded limited information. Furthermore, I possess an accessory mental foramen; I am curious if this might be connected to the aforementioned issues or if it is likely independent. I would be grateful for any clarification on these topics. Thank you in advance for your help!
Answers (1)
9/3/2025, 3:20:47 AM
OpenHealth AI
It's great that you're seeking to understand the potential connections between your spinal and renal anomalies. Your curiosity can help you better manage your conditions. Here's a breakdown of what you need to know:
Main Points
- Spinal and Renal Anomalies Correlation: There can be associations between spinal deformities and renal conditions like duplex kidneys.
- Accessory Mental Foramen: This is generally considered an anatomical variation and may not be directly related to the other conditions you've mentioned.
Explanation
Research suggests that some congenital anomalies can occur together due to shared developmental pathways during embryogenesis. Conditions like incomplete segmentation of spinal vertebrae and renal anomalies, such as duplex kidneys, can sometimes appear in the same person because of genetics or environmental factors that affect development. The correlation doesn’t imply direct causation; rather, it reflects overlapping developmental processes.
-
Incomplete Segmentation of C6 and C7: This finding often indicates a variation in spinal development. While it has not caused you complications yet, it's good to monitor any potential symptoms, especially as you age or if you experience increased spinal issues.
-
Duplex Kidney: This condition means you have an extra kidney that may or may not function normally. While it can be associated with other anatomical variations, many individuals live healthy lives with this condition.
-
Accessory Mental Foramen: This is a common variant of craniofacial anatomy and is often independent of spinal or renal anomalies. It usually does not cause issues unless it affects nerve pathways.
Next Steps
-
Routine Monitoring: Continue regular check-ups with a healthcare provider who understands your condition. This is important for early detection of any possible complications related to your spinal or renal health.
-
Keep Track of Symptoms: Maintain a journal of any new or worsening symptoms related to your spine or kidney function. This can help in discussions with your healthcare provider.
-
Research and Awareness: Continue educating yourself about hypermobile Ehlers-Danlos syndrome, as it may influence your spinal condition or overall health.
-
Connect with Support Groups: Consider joining a support group for individuals with Ehlers-Danlos syndrome or related conditions. Sharing experiences can provide insights and support.
Always feel free to reach out for more specific advice based on your ongoing experiences; it’s essential to address your concerns comprehensively. Remember, you are not alone in navigating these complex health issues!
Related Questions
Concerns About My Toes
Age: 30, Female Currently, I am on the lookout for a reputable podiatrist in my vicinity. However, I've encountered a perplexing issue with my foot. Just last night, I noticed a growth on the side of my toe, something entirely new to me. I maintain a nutritious diet and have a demanding job that requires me to be on my feet quite often. My footwear includes brands such as Brooks Ghost Runners, Hoka Bondi 9’s, and Nike Motiva’s, and I don’t opt for restrictive socks. I also apply Vick’s Vaporub to my feet, a practice handed down from my family, and stick with simple, non-fragrant lotions like Vanicream and CeraVe SA Cream for my skin. In addition, I am curious about the my big toenail's change in color. What might be the underlying reasons for this? Also, I have these persistent dark spots on my toes that I've struggled with since my days on the runway. Despite my efforts, nothing has succeeded in lightening or diminishing their appearance. I'm just looking to determine if there might have been a factor from the past that could have contributed to these issues. I’m not sure what else to include, but I’m open to answering any questions you might have. Thank you for your attention! Best wishes from a worried soul!
Strange Jelly-Like Substance Observed from Wound
I’m a 21-year-old female living with an auto-inflammatory condition known as hidradenitis suppurativa (HS). Recently, I've experienced a concerning issue with one of my wounds. This particular wound causes significant pain and excessive bleeding. However, whenever I attend to it, I tend to find this unusual jelly-like substance present within it. Interestingly, this phenomenon has only occurred with this one wound and not any of the others I have. The bleeding seems to persist until I manage to remove this jelly substance, after which it typically slows down and comes to a halt completely. I’m seeking insights into what this might signify so that I can effectively discuss it with my healthcare provider.
Battling Chronic Nausea and Vomiting for Over Two Years
For the past two years, I (age 26, female) have been enduring an incredibly challenging health situation. I experience intense nausea daily and find myself vomiting numerous times, with almost nothing providing relief. To provide some background, I’m from West Texas and I currently weigh around 190 pounds, standing at 5’7”. Initially, my weight was about 211 pounds when these symptoms began, and it fluctuates frequently between 190 and 225 pounds. I engage in vaping and consume THC. Previously diagnosed with hypothyroidism, my condition seemingly resolved, according to my healthcare providers. Additionally, I have polycystic ovarian syndrome (PCOS). I have consistently faced irregular bowel movements, with stools that are loose and sometimes appear to have mucus. Compounding my struggles, I've also suffered from migraines. I have had an IUD for over five years, experiencing two insertions of the Kyleena device. In December 2022, my battle with health took a severe turn when I was diagnosed with stage 4 Hodgkin’s Lymphoma, requiring chemotherapy treatment, specifically AVBD (Apologies for not recalling the exact medication names). By July 2023, I had fortunately achieved remission. However, after reaching remission, my vomiting worsened, transforming from primarily white foam to a mixture of 80% bile, any food I attempt to consume, and still white foam. This intense vomiting, accompanied by significant pain in my upper back, escalated to more than eight episodes daily by November 2023. At that time, THC seemed to be the only avenue for me to retain any food. During this tumultuous period, I consulted various doctors who, after confirming I wasn’t pregnant, attributed my symptoms to Cannabinoid Hyperemesis Syndrome (CHS). Immediately, I ceased THC consumption for over six months, yet the vomiting continued unabated. Each time, doctors would prescribe ondansetron, regardless of my claims that it provided no relief. I experimented with various diets recommended by medical professionals, but there were no improvements in my condition. Eventually, I obtained a referral to a gastroenterologist who intended to perform an endoscopy. However, the procedure was prohibitively expensive even with insurance, and thus was never conducted. This doctor also ordered blood tests to rule out several gastrointestinal disorders, such as Crohn's disease, Irritable Bowel Syndrome (IBS), and gluten sensitivity, but all results came back normal. Afterward, I had another appointment with a different gastroenterologist, but the doctor failed to meet with me. Instead, a nurse informed me that the doctor had merely recommended promethazine without conducting any tests or scheduling further visits. When I mentioned the possibility of gallbladder issues, the doctor laughed dismissively at my suggestion. Discussing my situation with my oncologist, he suggested that my heightened sensitivity to food odors stemmed from my chemotherapy experiences while I was working in fast food. While food smells indeed affect me, I'm primarily triggered by medical scents such as rubbing alcohol and cleaning agents. This ongoing ordeal has been overwhelmingly distressing. I now experience episodes of vomiting accompanied by bright red blood, presumably due to a throat tear. When I first encountered this troubling symptom, I consulted a doctor who appeared unfazed and prescribed a promethazine suppository, which does help but makes me extremely drowsy. My nausea persists nearly around the clock, often feeling as if there’s a heaviness in the upper part of my abdomen. I frequent urgent care facilities when my symptoms intensify, only to be met with minimal assistance since this is a chronic issue. Currently, I lack a primary care physician. Whenever I sought one, I encountered skepticism regarding my condition, with some healthcare professionals implying that I was exaggerating my symptoms. Though many physicians who do take my situation seriously seem baffled, I've lost count of the diverse medical experts I've consulted about these ongoing issues. If anyone has insight or suggestions, I would genuinely appreciate it. I can share my latest bloodwork results if that would be helpful—just let me know!
Strange Stomach Sensation Leading to Waking Up
Greetings. I'm a 36-year-old male, standing at 172 centimeters and weighing 90 kilograms. I don't take any medications, nor do I smoke. I've been living with diastasis recti for several years now, and I may also have irritable bowel syndrome (IBS). Additionally, I deal with fatty liver and kidney stones, though I assume these last two conditions are not related to my current concern. Occasionally, I experience a peculiar sensation that jolts me awake; it feels like a quick pulsing in my stomach. I’ve noticed it tends to affect the left side when I’m lying on my left side and the right side when on my right. Remarkably, it can occur even when I’m on my back. This strange feeling often escalates into a surge that fully rouses me. Alongside this, I sometimes feel prickling sensations throughout my body and fleeting lightheadedness. When this sensation disturbs my sleep while I’m turned to my side, shifting onto my back or the opposite side might alleviate it, but not always. In instances where I awaken while lying on my back, I discovered that gently pressing my hands on either side of my stomach can help, as can rising to a sitting or standing position. However, during my last two episodes—one a couple of weeks ago and another tonight—those techniques weren’t effective right away, which made me feel a bit anxious, prompting me to seek advice. Does anyone have insight into what might be going on? By the way, I’ve undergone routine ultrasound examinations of my abdomen by two different physicians during check-ups, both of whom assured me that everything appears normal, including my abdominal aorta and internal organs. They didn’t identify any issues at that time.
Healing Progress Post-GBS: Toe Concerns
I am a 28-year-old male, measuring 5 feet 10 inches and weighing 131 pounds. My current medications include Fomadatine and Zyrtec, prescribed due to my ongoing battle with Chronic Gastritis and SIBO. I maintain a healthy lifestyle, abstaining from both smoking and alcohol. My health concern revolves around the toe adjacent to my pinky toe on my left foot, as well as my pinky toe on the right foot. Since August of last year, I have been on the mend from Guillain Barre Syndrome. Recently, I've noticed that at night, the skin on my feet tends to turn a reddish pink, although this usually improves after I walk around. However, two of my toes have remained red, with one appearing slightly swollen. Generally, my pinky toes are quite thick, but the condition of my left foot's toe is worrisome for me. It seems that I'm unable to upload an image to illustrate my issue.