The following Conditions are related to Fingers

Select a specific condition below to view its details.

  • Apert syndrome

    Apert syndrome is a genetic condition that is present from birth. It involves the fusion of certain bones in the skull, which can cause problems with brain development and health. 1. There is no established or proven cure for Apert syndrome; however, there are treatments available to manage the symptoms. 2. In some cases, surgery can be used to correct the bones and facial deformities associated with the con  Read More

  • Bowen-conradi syndrome

    Bowen-Conradi syndrome, a highly uncommon hereditary condition, is marked by abnormalities of the head and face, developmental delays before birth, and infantile failure to thrive. Small head, prominent nose, small chin, minor joint limitation, clinodactyly, camptodactyly, foot deformities, and/or undescended testes (cryptorchidism) in afflicted males are some other physical anomalies. Kidney, brain, and/or other problems may  Read More

  • Coffin siris syndrome

    Multiple bodily systems are impacted by the illness known as Coffin-Siris syndrome. Developmental disability, anomalies of the fifth (pinky) fingers or toes, and distinctive facial features are trademarks of this disorder, despite the fact that there are numerous diverse signs and symptoms. 1. The majority of those affected have mild to severe intellectual disabilities or delayed speech and motor skill development  Read More

  • Duplication 9p syndrome

    Chromosome 9, Trisomy 9p is a rare chromosomal syndrome in which a portion of the 9th chromosome appears three times (trisomy) rather than twice in cells of the body. The trisomy may involve a portion of the short arm (9p), the entire short arm, or the short arm and a portion of the long arm (9q) of chromosome 9. (Each chromosome contains a short arm known as "p" and a long arm designated as "q.") Evidence suggests that, in many cases, associa  Read More

  • Ectrodactyly

    Ectrodactyly ectodermal dysplasia cleft lip/palate (EEC) syndrome is a rare genetic disorder. Symptoms can vary greatly from one person to another. Affected individuals often have abnormalities affecting the limbs including ectrodactyly, a condition in which part or all of the central digits (fingers or toes) are missing. Ectrodactyly often affects the middle fingers or toes, but can present differently in different people Ectrodactyly, which is  Read More

  • Escobar syndrome

    Depending on how severe the spinal deformities and webbing are, therapy is supportive. Here are some options for treating escobar syndrome: 1. Since scoliosis typically appears before the age of five in most individuals, orthopedic specialists must be consulted as soon as a diagnosis is obtained. 2. Plastic surgery in the regions of the webbing may be beneficial for patients with Escobar syndrome. Sub  Read More

  • Faciodigitogenital syndrome

    Since there is currently no permanent treatment for Facio Digito Genital syndrome, care is offered to enhance quality of life. A specialized team of healthcare professionals is needed to give a synchronized treatment for the patient's distinctive anomalies and associated symptoms: 1. Therapy of strabismus is used for disorders where the eyes are positioned erratically, impairing vision. In order to restore normal v  Read More

  • Fifth digit syndrome

    Fifth digit syndrome also known as Coffin-Siris syndrome is a genetic disorder that results in varying degrees of learning disability, developmental slowdowns, stunted 'pinky' toenails or fingernails, and distinctive facial features. Here are the risk factors for fifth digit syndrome: 1. The most common known cause of the condition is ARID1B gene variants. 2. The mode of inheritance is autosomal dominant, wh  Read More

  • Frontofacionasal dysostosis

    There's a partial cure available for frontofacionasal dysostosis. The treatment totally depends on the type of abnormality you're suffering from: 1. Bone malfunctions: Workout, vitamin and nutrient supplements, and drugs are used to treat established osteoporosis. Exercise and supplementation are frequently recommended to help prevent bone malfunctions. Other than that, at times surgeries are also recommended if t  Read More

  • Hart syndrome

    Hanhart syndrome is a rare birth defect in which the most obvious signs are a short, incompletely developed tongue (hypoglossia); absent or partially missing fingers and/or toes (hypodactylia); malformed arms and/or legs (peromelia); and an extremely small jaw (micrognathia). A more complete list of other signs frequently encountered may be found below. The severity of these physical abnormalities varies greatly from case to case. Children wit  Read More

  • Keratosis palmoplantaris transgradiens of siemens

    Keratosis planopilaris transgrediens of siemens is a genodermatosis characterized by hyperkeratosis. Initially, keratosis begins on the palm and soles and spreads to the dorsal aspects of hands, fingers, and feet as well as flexor aspects of wrists and heels. The skin manifestations set in by the age of 3 to 5 years. abnormal expression of structural proteins involved in the skin is the cause of the condition. Ris  Read More

  • Laband syndrome

    Laband syndrome, also known as Zimmerman-Laband syndrome, is an extremely rare genetic disorder characterized by abnormalities of the head and facial (craniofacial) area and the hands and feet. Most children with this disorder have abnormally large gums (gingival fibromatosis). Overgrown gums may affect the ability to chew, swallow, and/or speak. In addition, affected infants may exhibit abnormally long, thin fingers and toes and/or deformed (  Read More

  • Nager acrofacial dysostosis syndrome

    Nager Acrofacial Dysostosis Syndrome is a rare genetically inherited disorder where the newborn shows signs of craniofacial malformations. It's mostly associated with irregularities of the thumb and forearms. In particular circumstances, underdevelopment of bones in the face and hands is visible, while poor development of the cheek and jaw area is seen. Weak movement in the elbow is Cures/medications for Nager Acro  Read More

  • Odd syndrome

    Oculo-dento-digital dysplasia is a rare disorder that may be inherited as an autosomal dominant trait or be caused by a new change in the genes that occurs for no apparent reason (mutation). There also have been a few instances in which it is thought to have been inherited as an autosomal recessive trait. Major symptoms of cculo-dento-digital dysplasia are webbing of the fourth and fifth fingers, an abnormally small transparent part of the eye  Read More

  • Rubinstein taybi syndrome

    Rubinstein-Taybi Syndrome is a genetic disorder characterized by shortened stature, mild to severe intellectual disabilities, peculiar facial features, broader thumbs and first toes, abnormalities of the eyes, kidney and heart complications, dental issues, and obesity. The life expectancy of affected children does not exceed 5 years of age. Mutations of certain genes in the DNA are the primary cause, making it a ge  Read More

  • Split hand and split foot malformation

    Split hand/split foot malformation (SHFM) is a genetic disorder characterized by the complete or partial absence of some fingers or toes, often combined with clefts in the hands or feet. There may also be the appearance of webbing between fingers or toes (syndactyly). This may give the hands and/or feet a claw-like appearance. There are many types and combinations of deformities that appear in split hand/split foot malformation. Th  Read More

  • Split-hand and foot deformity

    Split hand/split foot malformation (SHFM) is a genetic disorder characterized by the complete or partial absence of some fingers or toes, often combined with clefts in the hands or feet. There may also be the appearance of webbing between fingers or toes (syndactyly). This may give the hands and/or feet a claw-like appearance. There are many types and combinations of deformities that appear in split hand/split foot malformation. Th  Read More

  • Syndactylic oxycephaly

    Mild cases of syndactylic oxycephaly may not require treatment. If the baby's cranial sutures are open and the skull is malformed, the doctor may recommend a specially designed helmet to assist correct the head. In this case, the molded helmet can help your baby's brain development and adjust the shape of the skull.However, surgery is the main treatment for the majority of newborns. The type and timing of surgery are det  Read More