A time-consuming and emotionally stressful adoption process can be immensely rewarding. When Christina Fisher of Florida met a couple who were interested in taking in her baby, Abigail Lynn, she decided to let them adopt. She discovered that she was born with treater Collins syndrome, a genetic condition that affects facial development. They decided not to proceed with the adoption. Christina Fisher found out she was pregnant and made the decision to give up the kid for adoption.
The mother from Florida was worried that she wouldn’t be able to provide her child with the attention it needed. The adoption agency was utilized by Mrs Fisher to locate the unidentified adoptive parents. Abigail Lynn was born with treasure Collin syndrome, an extremely rare condition. As a result, some of the most important features of her face were not fully formed.
The infant was not what she had expected, according to its adoptive mother, who fled the hospital. Ms Fisher opted to keep the baby and says she couldn’t imagine life without her. Her biological mother, Christina Fisher, has taken custody of Abigail Lynn, a five-month-old baby, and she’s currently living in Florida. Rather than being an unusual series of circumstances or an improbable tale, the truth behind Abigail’s reunion with her biological mother is both sad and wonderful.
Abigail Lynn was born on January 11, 2016, with treasured Collins syndrome, a condition that’s highly rare due to a genetic condition that resulted in Abigail’s facial structures not developing. As expected, her adoptive mother decided to abandon her and flee the hospital. Her birth mother took her in and now says she can’t imagine living without her daughter Abigail. A GoFundMe account was set up to help Ms Fisher care for Abigail and buy her baby clothes, diapers, wipes and other basic needs.
I spent the better part of last year pregnant and was going to give Abigail up for adoption. The creature of Collins syndrome that she was born with surprised us. It was not identified in the amniocentesis or the ultrasound, Miss Fisher wrote on the GoFundMe page. We never heard from her birth mother again. We’d left the hospital crying and expressing her disgust with her abnormality.
When the adoptive mother left the hospital in January 2016, she screamed and expressed how disfigured she was, and we haven’t heard from her since. I realized that she was only meant to be mine. Now, as a single mother with one daughter, Deborah, now 18, Ms Fisher decided to put Abigail up for adoption. There was no sign of the father, and the 36-year-old expecting mother was living in a trailer park nearing the conclusion of her pregnancy with the baby.
Her facial bones and tissue were affected from birth due to Abigail’s Treacher Collins syndrome, resulting in the underdevelopment of certain facial features like her cheekbones, ears and jaw. Abigail’s disability won’t keep her from enjoying a normal life, but her adoptive parents evidently couldn’t handle it. The adoption agency is said to have been taken aback by the adoptive parent’s reaction. Oxana Perry, a Florida-based photographer, recently had the pleasure of photographing Miss Fisher and her child. This has resulted in a wonderful collection of photos depicting the mother-daughter relationship, according to the GoFundMe website.
I was not prepared for her, Abigail, but now I cannot fathom life without either of my kids, Miss Fisher says at the end of her Poignant GoFundMe page. Thanks to everyone who’s helped, I want to extend my gratitude to you all, the mother says. Treat your Collins syndrome is a disorder that disrupts the development of the Face, bones, and tissues. Edward Treacher Collins, a Londonoptimal biologist who first documented the illness in medical literature in 1900, is the name of the syndrome. The signs and symptoms of the disorder can range from hardly apparent to severe.
The majority of those affected have undeveloped facial bones, especially cheap bones, as well as a tiny jaw and chin. Some persons with this condition are born with a cleft palate, which is an opening in the roof of the mouth. Sufferers have major life-threatening respiratory problems and severe circumstances. Treat your colon syndrome, or TCS is a rare genetic condition marked by severe head and facial deformities. Under the development of the Zygomatic complex.
Cheekbones, jaws, palate, and mouth are common in craniofacial abnormalities, which can cause respiratory and feeding problems. Affected people may also have eye malformations, such as a downward slant of the aperture between the upper and lower eyelids and anomalies of the external and middle ear structures, which can cause hearing loss. Microcephaly and psychomotor slowness are two brain and behavioural defects that have been documented as part of the disorder. These symptoms and physical traits differ considerably from one person to the next. Some people may go undiagnosed because they’re only minimally affected, while others may suffer major life-threatening consequences.
Changes or mutations in the TCOFone gene are the most common cause of TCS, but they can also be caused by mutations in the PorB porc or portioned genes. Tcof One and Por One B have autosomal dominant inheritance, but Por One C has an autosomal recessive inheritance. Po LR 1D mutations, on the other hand, have been linked to TCS in both autosomal dominant and recessive forms. These symptoms and severity can differ considerably from one individual to the next, even within the same family. Some people may be undetected because their symptoms are so minor.
Others may have major abnormalities and the risk of life-threatening respiratory problems. It’s crucial to note that not everyone who is impacted may experience all of the symptoms listed. This affects the bones of the face, the ears, and the soft tissues around the eyes, among other things. Individuals with the condition have distinct facial traits and may develop hearing and vision impairments. This is characterized by symmetrical, nearly similar facial deformities that are present at birth.
The congenital hearing loss left palate, or jaw and airway difficulties can all affect speech and language development, although intelligence is normally unaffected. Neurological and behavioural abnormalities such as microcephaly and cognitive delay, have been documented as part of the illness. On a rare basis, TCS causes the cheekbones to be underdeveloped or missing, making the area of the face appear flat or sunken.
Mandibular hypoplasia is a condition in which the lower Jawbone is not fully grown, causing the chin and lower jaw to seem abnormally tiny. Certain bony structures that anchor sections of the lower jaw bone to muscle might be unusually flat or missing.
Affected infants may also have throat underdevelopment. Early infancy, eating problems, and or breathing difficulties may be caused by pharyngeal hypoplasia with underdevelopment of the lower jaw and or abnormal smallness of the jaw. Obstructive sleep apnea, which is characterized by recurrent, short pauses of regular breathing, and air movement during sleep, can affect children. Life-threatening breathing issues may arise in certain seriously affected people. Use the search term infantile apnea in the Rare Disease Database to learn more about this disorder.
Narrowing or occlusion of the nasal Airways is the further anomaly that may contribute to respiratory or eating issues. Severe micrognathia, a tongue that shifted farther back in the mouth than normal, and inadequate closure of the roof of the mouth are all characteristics of the Pierre Robin sequence. In some children, even when the palate unites, it can still be excessively arched, causing problems with eating and breathing.
Dental anomalies such as undeveloped or hypoplastic and or misplaced teeth can also be caused by deformities of the mouth and jaw. Missing teeth, clouding or darkening in the teeth, and inappropriate eruption of certain upper teeth are among the other dental anomalies described.
Due to the failure of sound waves to pass through the middle ear, people with TCS may acquire hearing loss. Individuals with TCS may also have deformed or nonexistent obstacles. The three small bones through which sound waves are transferred in the middle ear as a result of anomalies affecting structures within the middle ear. Furthermore, the external ear structures are frequently nonexistent, tiny or deformed, and the external ear canals are narrowed or blocked. Crumpled or rotated outer ears are common.
The inner ear, on the other hand, is normally unharmed, though male formations of the inner ears, bony spiral organs or cochlea, and balance-related structures have been documented. Additional symptoms include the presence of tiny skin growths or pits right in front of the external ear and an irregular tube that drains the ears to the nose but is closed on one end.
This causes problem in the tissue surrounding the eyes, and many babies. Affected individuals may have a melancholy facial appearance as a result of their eye abnormalities. A downward tilt to the aperture between the upper and lower eyelids is the most prevalent ocular symptom.
A lower eyelid gap or cleft of missing lid tissue, partial lack of lower eyelashes, crossed eyes, and constricted tear ducts are further signs. Malformations of the globe are occasionally found and might include a notch or cleft of missing Iris tissue. As well as abnormally small eyes. Some patients may experience vision loss. The severity and combination of ocular defects determine the degree of vision impairment.
